| geneid | 16 |
|---|---|
| ensemblid | ENSG00000090861.17 |
| hgncid | 20 |
| symbol | AARS1 |
| name | alanyl-tRNA synthetase 1 |
| refseq_nuc | NM_001605.3 |
| refseq_prot | NP_001596.2 |
| ensembl_nuc | ENST00000261772.13 |
| ensembl_prot | ENSP00000261772.8 |
| mane_status | MANE Select |
| chr | chr16 |
| start | 70252298 |
| end | 70289506 |
| strand | - |
| ver | v1.2 |
| region | chr16:70252298-70289506 |
| region5000 | chr16:70247298-70294506 |
| regionname0 | AARS1_chr16_70252298_70289506 |
| regionname5000 | AARS1_chr16_70247298_70294506 |
| chr:pos | ref | alt | af | annotation | impact | samples | AHAPIDS | ACHAPIDS | ACTHAPIDS | ACTGHAPIDS | ac | an | len | genename | geneid | featuretype | featureid | transcript_biotype | rank | hgvs_c | hgvs_p | cdna_pos_length | cds_pos_length | aa_pos_length | distance | status |
|---|
| genename | grch38/chm13v2 1/0: The haplotype type is the same as GRCh380/1: The haplotype type is the same as CHM13v20/0: The haplotype type matches neither GRCh38 nor CHM13v21/1: The haplotype type is the same on both GRCh38 and CHM13v2
|
ahapid | alen | total | AFR | AMR | EAS | EUR | SAS | aseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| AARS1 | 1/1 | a0001 | 968 | 325 | 52 | 72 | 147 | 14 | 38 | subcellular location copy fasta | chr16 | 70247298 | 70294506 |
Click to load Haplotype QTL data...
| pos | S. Strand |
E# Exon Number |
max | median | min | diff | type | haplotypeid | max_hap_list | min_hap_list | symbol | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70282620 | - | 2 | -0.9996 | -0.9996 | -0.9996 | 0.0001 | acceptor | a0001 | HG00099.hp1 HG01071.hp1 HG01433.hp1 HG03490.hp1 HG03516.hp1 others(5): Show |
HG02055.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70282784 | - | 2 | 0.9987 | 0.9987 | 0.9985 | 0.0002 | donor | a0001 | HG01106.hp2 | HG00597.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| 70276966 | - | 3 | -0.9993 | -0.9993 | -0.9992 | 0.0001 | acceptor | a0001 | NA19079.hp2 | HG02148.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| 70277154 | - | 3 | 0.9957 | 0.9951 | 0.9946 | 0.0010 | donor | a0001 | HG02027.hp1 | NA19062.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| 70276486 | - | 4 | -0.9979 | -0.9978 | -0.9974 | 0.0005 | acceptor | a0001 | HG02055.hp2 | HG01993.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70276631 | - | 4 | 0.9988 | 0.9984 | 0.9982 | 0.0005 | donor | a0001 | HG02896.hp1 NA19078.hp2 |
NA18998.hp2 NA19082.hp2 NA19090.hp2 |
AARS1 | chr16 | 70247298 | 70294506 |
| 70271781 | - | 5 | -0.9976 | -0.9972 | -0.9966 | 0.0010 | acceptor | a0001 | NA19077.hp2 | HG02647.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| 70271972 | - | 5 | 0.9965 | 0.9960 | 0.9954 | 0.0012 | donor | a0001 | HG02071.hp2 NA18954.hp2 |
NA18998.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70270196 | - | 6 | -0.9731 | -0.9654 | -0.9596 | 0.0135 | acceptor | a0001 | NA18994.hp2 | NA18978.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70270340 | - | 6 | 0.8381 | 0.8118 | 0.8020 | 0.0361 | donor | a0001 | NA18994.hp2 | HG02486.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70269618 | - | 7 | -0.9990 | -0.9987 | -0.9986 | 0.0004 | acceptor | a0001 | HG02055.hp2 | NA18952.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70269763 | - | 7 | 0.9976 | 0.9974 | 0.9965 | 0.0010 | donor | a0001 | HG00099.hp2 HG00140.hp2 HG01070.hp2 HG01071.hp2 HG01074.hp1 others(20): Show |
NA18971.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| 70268271 | - | 8 | -0.9973 | -0.9968 | -0.9963 | 0.0010 | acceptor | a0001 | HG01884.hp2 | HG01261.hp2 HG02148.hp2 |
AARS1 | chr16 | 70247298 | 70294506 |
| 70268379 | - | 8 | 0.9941 | 0.9935 | 0.9923 | 0.0018 | donor | a0001 | HG00423.hp1 | NA18966.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| 70267659 | - | 9 | -0.9994 | -0.9993 | -0.9993 | 0.0001 | acceptor | a0001 | HG03139.hp2 NA20129.hp1 |
HG01074.hp1 HG02257.hp1 HG04184.hp1 NA18966.hp1 |
AARS1 | chr16 | 70247298 | 70294506 |
| 70267809 | - | 9 | 0.9986 | 0.9985 | 0.9984 | 0.0002 | donor | a0001 | HG00280.hp2 | HG03139.hp2 NA20129.hp1 |
AARS1 | chr16 | 70247298 | 70294506 |
| 70265538 | - | 10 | -0.9982 | -0.9980 | -0.9970 | 0.0012 | acceptor | a0001 | HG03017.hp1 | HG04184.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| 70265662 | - | 10 | 0.9986 | 0.9984 | 0.9976 | 0.0010 | donor | a0001 | HG00140.hp1 HG01256.hp2 HG02015.hp2 HG04115.hp1 HG04199.hp2 others(2): Show |
HG02257.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| 70264958 | - | 11 | -0.9975 | -0.9971 | -0.9969 | 0.0006 | acceptor | a0001 | HG04184.hp1 | HG04204.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| 70265102 | - | 11 | 0.9946 | 0.9938 | 0.9932 | 0.0013 | donor | a0001 | HG00140.hp1 HG01256.hp2 HG04199.hp2 NA18952.hp2 |
HG04204.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| 70262346 | - | 12 | -0.9937 | -0.9911 | -0.9880 | 0.0057 | acceptor | a0001 | HG02015.hp2 | NA19057.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70262524 | - | 12 | 0.9936 | 0.9866 | 0.9810 | 0.0126 | donor | a0001 | HG02015.hp2 | NA19057.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70261044 | - | 13 | -0.9946 | -0.9939 | -0.9934 | 0.0012 | acceptor | a0001 | HG03831.hp1 | NA19082.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70261157 | - | 13 | 0.9967 | 0.9964 | 0.9961 | 0.0006 | donor | a0001 | NA18975.hp1 | HG00438.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70258980 | - | 14 | -0.9889 | -0.9882 | -0.9804 | 0.0085 | acceptor | a0001 | NA18978.hp1 | NA18983.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70259186 | - | 14 | 0.9897 | 0.9881 | 0.9846 | 0.0051 | donor | a0001 | NA18969.hp2 | NA18983.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70258033 | - | 15 | -0.8823 | -0.8741 | -0.8612 | 0.0211 | acceptor | a0001 | NA18966.hp2 | HG02257.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70258217 | - | 15 | 0.9189 | 0.9050 | 0.8920 | 0.0268 | donor | a0001 | HG01069.hp2 HG01070.hp1 HG01952.hp2 HG02083.hp2 HG02135.hp2 others(2): Show |
HG02109.hp1 HG02451.hp1 HG02486.hp2 HG02717.hp2 HG03540.hp2 |
AARS1 | chr16 | 70247298 | 70294506 |
| 70255728 | - | 16 | -0.9983 | -0.9979 | -0.9974 | 0.0009 | acceptor | a0001 | NA18966.hp2 | NA18944.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70255836 | - | 16 | 0.9960 | 0.9952 | 0.9944 | 0.0015 | donor | a0001 | NA18966.hp2 | HG00558.hp1 HG01071.hp1 HG02015.hp1 HG02040.hp1 HG02080.hp1 others(18): Show |
AARS1 | chr16 | 70247298 | 70294506 |
| 70254621 | - | 17 | -0.9966 | -0.9966 | -0.9961 | 0.0005 | acceptor | a0001 | HG00733.hp1 HG01358.hp2 HG01496.hp2 HG01952.hp1 HG02027.hp1 others(24): Show |
HG04184.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| 70254734 | - | 17 | 0.9974 | 0.9973 | 0.9970 | 0.0005 | donor | a0001 | NA18954.hp2 NA18971.hp1 NA18988.hp2 |
NA18966.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70253919 | - | 18 | -0.9990 | -0.9989 | -0.9988 | 0.0001 | acceptor | a0001 | HG02055.hp2 HG03139.hp2 NA20129.hp1 |
HG00741.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70254038 | - | 18 | 0.9981 | 0.9980 | 0.9980 | 0.0001 | donor | a0001 | HG00741.hp2 | HG04184.hp1 NA19240.hp2 |
AARS1 | chr16 | 70247298 | 70294506 |
| 70253714 | - | 19 | -0.7711 | -0.7642 | -0.7491 | 0.0221 | acceptor | a0001 | HG00741.hp2 | HG01943.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70253800 | - | 19 | 0.9979 | 0.9979 | 0.9970 | 0.0009 | donor | a0001 | HG00639.hp2 HG01106.hp1 HG01109.hp2 HG01257.hp1 HG01516.hp2 others(4): Show |
HG01943.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70253268 | - | 20 | -0.9977 | -0.9968 | -0.9967 | 0.0010 | acceptor | a0001 | HG02055.hp2 HG03139.hp2 NA20129.hp1 |
NA18993.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| 70253381 | - | 20 | 0.9951 | 0.9944 | 0.9943 | 0.0007 | donor | a0001 | HG02055.hp2 HG03139.hp2 NA20129.hp1 |
NA18966.hp2 | AARS1 | chr16 | 70247298 | 70294506 |
| 70252906 | - | 21 | 0.9929 | 0.9923 | 0.9920 | 0.0009 | donor | a0001 | HG00741.hp2 | NA19068.hp1 | AARS1 | chr16 | 70247298 | 70294506 |
| pos | annotationhgvs_chgvs_p | clinvarid | clnsig | geneinfo | mc | clndisdb | strand strand
|
ahapid ahapid_count
|
chapid chapid count
|
thapid thapid_count
|
ghapid ghapid_count
|
AHAPIDS ahapids
|
ACHAPIDS achapids
|
ACTHAPIDS acthapids
|
ACTGHAPIDS actghapids
|
haplotypeids haplotypeids
|
impact | chr | ref | alt | external |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 70289413:splice 70289413:variant goto | c.-22+8G>A | 513796 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:CN169374 | - | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0003 | HG03710.hp2 | LOW | chr16 | C | T | TogoVar |
| 70253274:splice 70253274:variant goto | c.2715T>Cp.Val905Val | 320325 | Benign | AARS1:16 | SO:0001819 synonymous_variant |
MONDO:MONDO:0018993 MedGen:C0270914 Orphanet:64746|MedGen:CN169374|MONDO:MONDO:0014593 MedGen:C4225361 OMIM:616339 others(4): Show |
- | 10 | 16 | 23 | 321 | a0001a0002a0003a0005a0006others(5): Show | a0001c0001a0001c0002a0001c0007a0001c0010a0001c0013others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006a0001c0001t0007a0001c0001t0008others(18): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(316): Show | HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(318): Show |
LOW | chr16 | A | G | TogoVar |
| 70258841:splice 70258841:variant goto | c.1992+139A>G | 1230605 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 10 | 16 | 23 | 321 | a0001a0002a0003a0005a0006others(5): Show | a0001c0001a0001c0002a0001c0007a0001c0010a0001c0013others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006a0001c0001t0007a0001c0001t0008others(18): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(316): Show | HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(318): Show |
MODIFIER | chr16 | T | C | TogoVar |
| 70269677:splice 70269677:variant goto | c.903C>Tp.His301His | 287973 | Benign | AARS1:16 | SO:0001819 synonymous_variant |
MONDO:MONDO:0013212 MedGen:C2750090 OMIM:613287 Orphanet:228174|MedGen:CN169374|MONDO:MONDO:0018993 MedGen:C0270914 others(1): Show |
- | 5 | 8 | 12 | 161 | a0001a0006a0007a0009a0010 | a0001c0001a0001c0007a0001c0013a0001c0016a0006c0018others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006a0001c0001t0007a0001c0001t0008others(7): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(156): Show | HG00280.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
LOW | chr16 | G | A | TogoVar |
| 70289223:splice 70289223:variant goto | c.-22+198G>A | 1248821 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 5 | 8 | 10 | 144 | a0001a0006a0007a0009a0010 | a0001c0001a0001c0007a0001c0013a0001c0016a0006c0018others(3): Show | a0001c0001t0001a0001c0001t0006a0001c0001t0007a0001c0007t0001a0001c0013t0001others(5): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(139): Show | HG00280.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp1 HG00423.hp2 others(139): Show |
MODIFIER | chr16 | C | T | TogoVar |
| 70282331:splice 70282331:variant goto | c.144+288dupT | 1241551 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 10 | 17 | 23 | 315 | a0001a0002a0003a0004a0005others(5): Show | a0001c0001a0001c0002a0001c0003a0001c0007a0001c0010others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006a0001c0001t0007a0001c0001t0008others(18): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(310): Show | HG00099.hp2 HG00140.hp1 HG00140.hp2 HG00280.hp1 HG00280.hp2 others(312): Show |
MODIFIER | chr16 | G | GA | TogoVar |
| 70258895:splice 70258895:variant goto | c.1992+83_1992+84delCT | 1250942 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:CN169374|MedGen:C3661900 | - | 2 | 6 | 7 | 89 | a0001a0010 | a0001c0001a0001c0002a0001c0007a0001c0013a0001c0016others(1): Show | a0001c0001t0001a0001c0001t0007a0001c0002t0001a0001c0007t0001a0001c0013t0001others(2): Show | a0001c0001t0001g0003a0001c0001t0001g0017a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0044others(84): Show | HG00280.hp1 HG00280.hp2 HG00323.hp1 HG00438.hp1 HG00558.hp2 others(84): Show |
MODIFIER | chr16 | CAG | C | TogoVar |
| 70268131:splice 70268131:variant goto | c.1071+140C>A | 1236014 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 2 | 5 | 6 | 91 | a0001a0010 | a0001c0001a0001c0007a0001c0013a0001c0016a0010c0014 | a0001c0001t0001a0001c0001t0007a0001c0007t0001a0001c0013t0001a0001c0016t0001others(1): Show | a0001c0001t0001g0003a0001c0001t0001g0038a0001c0001t0001g0040a0001c0001t0001g0044a0001c0001t0001g0045others(86): Show | HG00280.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp2 HG00438.hp1 others(86): Show |
MODIFIER | chr16 | G | T | TogoVar |
| 70269515:splice 70269515:variant goto | c.962+103G>A | 1280284 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 22 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0039a0001c0001t0001g0041others(17): Show | HG00738.hp1 HG01243.hp1 HG02486.hp1 HG02572.hp1 HG02615.hp1 others(17): Show |
MODIFIER | chr16 | C | T | TogoVar |
| 70265953:splice 70265953:variant goto | c.1223-291G>A | 1179274 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 5 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0042a0001c0001t0001g0059 | HG02809.hp1 HG02818.hp1 HG03471.hp1 HG03579.hp1 HG06807.hp2 |
MODIFIER | chr16 | C | T | TogoVar |
| 70271703:splice 70271703:variant goto | c.671+78C>T | 1200390 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 4 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0035a0001c0001t0001g0036a0001c0001t0001g0037a0001c0001t0001g0059 | HG02818.hp1 HG03471.hp1 HG03579.hp1 HG06807.hp2 |
MODIFIER | chr16 | G | A | TogoVar |
| 70261257:splice 70261257:variant goto | c.1672-100T>C | 1211108 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0041 | HG03516.hp1 | MODIFIER | chr16 | A | G | TogoVar |
| 70253810:splice 70253810:variant goto | c.2521-10T>C | 386600 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900|MONDO:MONDO:0018993 MedGen:C0270914 Orphanet:64746 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0094 | HG00741.hp2 | MODIFIER | chr16 | A | G | TogoVar |
| 70268136:splice 70268136:variant goto | c.1071+135G>T | 1258369 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0096 | HG00280.hp2 | MODIFIER | chr16 | C | A | TogoVar |
| 70276240:splice 70276240:variant goto | c.479+246T>A | 672497 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0144 | HG01081.hp2 | MODIFIER | chr16 | A | T | TogoVar |
| 70265687:splice 70265687:variant goto | c.1223-26dupT | 1290871 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 2 | 4 | 4 | 23 | a0001a0008 | a0001c0001a0001c0002a0001c0010a0008c0011 | a0001c0001t0001a0001c0002t0001a0001c0010t0001a0008c0011t0001 | a0001c0001t0001g0166a0001c0002t0001g0165a0001c0002t0001g0184a0001c0002t0001g0201a0001c0002t0001g0207others(18): Show | HG00140.hp1 HG00323.hp2 HG00438.hp2 HG01256.hp2 HG01346.hp1 others(18): Show |
MODIFIER | chr16 | C | CA | TogoVar |
| 70252647:splice 70252647:variant goto | c.*74A>T | 320323 | Benign | AARS1:16 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0013212 MedGen:C2750090 OMIM:613287 Orphanet:228174|MedGen:C3661900 |
- | 1 | 1 | 2 | 14 | a0001 | a0001c0001 | a0001c0001t0002a0001c0001t0008 | a0001c0001t0002g0164a0001c0001t0002g0167a0001c0001t0002g0179a0001c0001t0002g0180a0001c0001t0002g0243others(9): Show | HG00639.hp2 HG01106.hp1 HG01109.hp2 HG01123.hp2 HG01257.hp1 others(9): Show |
MODIFIER | chr16 | T | A | TogoVar |
| 70257903:splice 70257903:variant goto | c.2177+130A>G | 1178488 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 2 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0243a0001c0001t0002g0310 | HG02257.hp2 HG02717.hp1 |
MODIFIER | chr16 | T | C | TogoVar |
| 70255554:splice 70255554:variant goto | c.2286+174A>G | 1190737 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 3 | 7 | a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0003a0001c0002t0004 | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324others(2): Show | HG02055.hp2 HG02109.hp1 HG02451.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
MODIFIER | chr16 | T | C | TogoVar |
| 70262692:splice 70262692:variant goto | c.1493-168C>T | 1195470 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 3 | 7 | a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0003a0001c0002t0004 | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324others(2): Show | HG02055.hp2 HG02109.hp1 HG02451.hp1 HG02486.hp2 HG02717.hp2 others(3): Show |
MODIFIER | chr16 | G | A | TogoVar |
| 70261362:splice 70261362:variant goto | c.1672-205G>C | 677700 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 4 | 4 | 6 | 36 | a0001a0002a0003a0005 | a0001c0002a0002c0004a0003c0005a0005c0009 | a0001c0002t0001a0001c0002t0003a0001c0002t0004a0002c0004t0001a0003c0005t0001others(1): Show | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324others(31): Show | HG01433.hp2 HG02055.hp2 HG02109.hp1 HG02109.hp2 HG02258.hp2 others(32): Show |
MODIFIER | chr16 | C | G | TogoVar |
| 70262711:splice 70262711:variant goto | c.1493-187T>C | 677699 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 4 | 4 | 6 | 36 | a0001a0002a0003a0005 | a0001c0002a0002c0004a0003c0005a0005c0009 | a0001c0002t0001a0001c0002t0003a0001c0002t0004a0002c0004t0001a0003c0005t0001others(1): Show | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324others(31): Show | HG01433.hp2 HG02055.hp2 HG02109.hp1 HG02109.hp2 HG02258.hp2 others(32): Show |
MODIFIER | chr16 | A | G | TogoVar |
| 70265517:splice 70265517:variant goto | c.1347+21A>G | 675695 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 4 | 4 | 6 | 36 | a0001a0002a0003a0005 | a0001c0002a0002c0004a0003c0005a0005c0009 | a0001c0002t0001a0001c0002t0003a0001c0002t0004a0002c0004t0001a0003c0005t0001others(1): Show | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324others(31): Show | HG01433.hp2 HG02055.hp2 HG02109.hp1 HG02109.hp2 HG02258.hp2 others(32): Show |
MODIFIER | chr16 | T | C | TogoVar |
| 70268430:splice 70268430:variant goto | c.963-51A>C | 673419 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 4 | 4 | 6 | 36 | a0001a0002a0003a0005 | a0001c0002a0002c0004a0003c0005a0005c0009 | a0001c0002t0001a0001c0002t0003a0001c0002t0004a0002c0004t0001a0003c0005t0001others(1): Show | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324others(31): Show | HG01433.hp2 HG02055.hp2 HG02109.hp1 HG02109.hp2 HG02258.hp2 others(32): Show |
MODIFIER | chr16 | T | G | TogoVar |
| 70262752:splice 70262752:variant goto | c.1493-228C>T | 677698 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 3 | 3 | 5 | 32 | a0001a0002a0005 | a0001c0002a0002c0004a0005c0009 | a0001c0002t0001a0001c0002t0003a0001c0002t0004a0002c0004t0001a0005c0009t0001 | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324others(27): Show | HG01433.hp2 HG02055.hp2 HG02109.hp1 HG02109.hp2 HG02258.hp2 others(28): Show |
MODIFIER | chr16 | G | A | TogoVar |
| 70254829:splice 70254829:variant goto | c.2287-95A>G | 676184 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 4 | 4 | 6 | 33 | a0001a0002a0003a0005 | a0001c0002a0002c0004a0003c0005a0005c0009 | a0001c0002t0001a0001c0002t0003a0001c0002t0004a0002c0004t0001a0003c0005t0001others(1): Show | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324others(28): Show | HG01433.hp2 HG02055.hp2 HG02109.hp1 HG02109.hp2 HG02258.hp2 others(29): Show |
MODIFIER | chr16 | T | C | TogoVar |
| 70258791:splice 70258791:variant goto | c.1992+189C>T | 1220233 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 2 | 4 | a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0004 | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0004g0149a0001c0002t0004g0150 | HG02109.hp1 HG02451.hp1 HG02486.hp2 HG02717.hp2 HG03540.hp2 |
MODIFIER | chr16 | G | A | TogoVar |
| 70258798:splice 70258798:variant goto | c.1992+181delG | 1213501 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 2 | 4 | a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0004 | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0004g0149a0001c0002t0004g0150 | HG02109.hp1 HG02451.hp1 HG02486.hp2 HG02717.hp2 HG03540.hp2 |
MODIFIER | chr16 | GC | G | TogoVar |
| 70269600:splice 70269600:variant goto | c.962+18T>C | 381159 | Benign | AARS1:16 | SO:0001627 intron_variant |
MONDO:MONDO:0018993 MedGen:C0270914 Orphanet:64746|MedGen:C3661900|MedGen:CN169374 |
- | 1 | 1 | 2 | 4 | a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0004 | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0004g0149a0001c0002t0004g0150 | HG02109.hp1 HG02451.hp1 HG02486.hp2 HG02717.hp2 HG03540.hp2 |
MODIFIER | chr16 | A | G | TogoVar |
| 70271512:splice 70271512:variant goto | c.671+269C>G | 1198285 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 2 | 4 | a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0004 | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0004g0149a0001c0002t0004g0150 | HG02109.hp1 HG02451.hp1 HG02486.hp2 HG02717.hp2 HG03540.hp2 |
MODIFIER | chr16 | G | C | TogoVar |
| 70272040:splice 70272040:variant goto | c.480-68G>A | 1178436 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 2 | 4 | a0001 | a0001c0002 | a0001c0002t0001a0001c0002t0004 | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0004g0149a0001c0002t0004g0150 | HG02109.hp1 HG02451.hp1 HG02486.hp2 HG02717.hp2 HG03540.hp2 |
MODIFIER | chr16 | C | T | TogoVar |
| 70265789:splice 70265789:variant goto | c.1223-144_1223-128delTGGATTTTCTGATGGGC | 676230 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:CN517202 | - | 1 | 1 | 1 | 38 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0002a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0161others(33): Show | HG00099.hp2 HG00140.hp2 HG01070.hp2 HG01071.hp2 HG01074.hp1 others(34): Show |
MODIFIER | chr16 | TGCCCATC others(10): Show |
T | TogoVar |
| 70265752:splice 70265752:variant goto | c.1223-90C>T | 1212926 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0192a0001c0002t0001g0258 | HG01074.hp1 HG02257.hp1 |
MODIFIER | chr16 | G | A | TogoVar |
| 70272279:splice 70272279:variant goto | c.480-307G>A | 1205294 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 2 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0216a0001c0002t0001g0295 | HG01069.hp1 HG01071.hp1 |
MODIFIER | chr16 | C | T | TogoVar |
| 70262534:splice 70262534:variant goto | c.1493-10C>T | 703013 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MONDO:MONDO:0018993 MedGen:C0270914 Orphanet:64746 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0238 | HG02015.hp2 | MODIFIER | chr16 | G | A | TogoVar |
| 70289507:splice 70289507:variant goto | c.-108T>C | 320357 | Uncertain_significance | AARS1:16 | . | MONDO:MONDO:0013212 MedGen:C2750090 OMIM:613287 Orphanet:228174 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0246 | HG00642.hp2 | MODIFIER | chr16 | A | G | TogoVar |
| 70264731:splice 70264731:variant goto | c.1492+226dupA | 1183457 | Benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 4 | 4 | 5 | 23 | a0001a0002a0003a0005 | a0001c0002a0002c0004a0003c0005a0005c0009 | a0001c0002t0001a0001c0002t0003a0002c0004t0001a0003c0005t0001a0005c0009t0001 | a0001c0002t0001g0262a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324a0002c0004t0001g0335others(18): Show | HG01433.hp2 HG02055.hp2 HG02109.hp2 HG02451.hp2 HG02572.hp2 others(18): Show |
MODIFIER | chr16 | A | AT | TogoVar |
| 70251882:splice 70251882:variant goto | c.*839C>G | 4020525 | Uncertain_significance | EXOSC6:118460 | SO:0001583 missense_variant |
MedGen:CN169374 | - | 1 | 1 | 1 | 1 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0277 | NA19057.hp1 | MODIFIER | chr16 | G | C | TogoVar |
| 70252470:splice 70252470:variant goto | c.*251A>C | 320320 | Benign/Likely_benign | AARS1:16 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0013212 MedGen:C2750090 OMIM:613287 Orphanet:228174|MedGen:C3661900 |
- | 1 | 1 | 1 | 3 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324 | HG02055.hp2 HG03139.hp2 NA20129.hp1 |
MODIFIER | chr16 | T | G | TogoVar |
| 70253037:splice 70253037:variant goto | c.2722-133_2722-132delAA | 1218123 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 3 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324 | HG02055.hp2 HG03139.hp2 NA20129.hp1 |
MODIFIER | chr16 | CTT | C | TogoVar |
| 70264656:splice 70264656:variant goto | c.1492+302C>A | 1180908 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 3 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324 | HG02055.hp2 HG03139.hp2 NA20129.hp1 |
MODIFIER | chr16 | G | T | TogoVar |
| 70268073:splice 70268073:variant goto | c.1071+195_1071+197delCCT | 1199673 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 3 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324 | HG02055.hp2 HG03139.hp2 NA20129.hp1 |
MODIFIER | chr16 | CAGG | C | TogoVar |
| 70276290:splice 70276290:variant goto | c.479+196T>A | 1189850 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 3 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324 | HG02055.hp2 HG03139.hp2 NA20129.hp1 |
MODIFIER | chr16 | A | T | TogoVar |
| 70276291:splice 70276291:variant goto | c.479+195C>A | 1216215 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 3 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324 | HG02055.hp2 HG03139.hp2 NA20129.hp1 |
MODIFIER | chr16 | G | T | TogoVar |
| 70283063:splice 70283063:variant goto | c.-21-279G>A | 1198623 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 3 | a0001 | a0001c0002 | a0001c0002t0003 | a0001c0002t0003g0322a0001c0002t0003g0323a0001c0002t0003g0324 | HG02055.hp2 HG03139.hp2 NA20129.hp1 |
MODIFIER | chr16 | C | T | TogoVar |
| 70252508:splice 70252508:variant goto | c.*213C>T | 320321 | Likely_benign | AARS1:16 | SO:0001624 3_prime_UTR_variant |
MONDO:MONDO:0013212 MedGen:C2750090 OMIM:613287 Orphanet:228174 |
- | 1 | 1 | 1 | 2 | a0001 | a0001c0002 | a0001c0002t0004 | a0001c0002t0004g0149a0001c0002t0004g0150 | HG02109.hp1 HG02451.hp1 |
MODIFIER | chr16 | G | A | TogoVar |
| 70289294:splice 70289294:variant goto | c.-22+127G>A | 1187804 | Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MedGen:C3661900 | - | 1 | 1 | 1 | 2 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0004a0001c0003t0001g0005 | HG01496.hp1 HG03017.hp2 |
MODIFIER | chr16 | C | T | TogoVar |
| 70258221:splice 70258221:variant goto | c.1993-4G>A | 508300 | Benign/Likely_benign | AARS1:16 | SO:0001627 intron_variant |
MONDO:MONDO:0018993 MedGen:C0270914 Orphanet:64746|MedGen:CN169374 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0003 | a0001c0003t0001 | a0001c0003t0001g0284 | HG02698.hp2 | LOW | chr16 | C | T | TogoVar |
| 70268298:splice 70268298:variant goto | c.1044G>Cp.Thr348Thr | 282997 | Benign/Likely_benign | AARS1:16 | SO:0001819 synonymous_variant |
MONDO:MONDO:0013212 MedGen:C2750090 OMIM:613287 Orphanet:228174|MedGen:CN169374|MeSH:D030342 MedGen:C0950123|MONDO:MONDO:0018993 others(9): Show |
- | 1 | 1 | 1 | 2 | a0001 | a0001c0007 | a0001c0007t0001 | a0001c0007t0001g0070a0001c0007t0001g0092 | HG01261.hp2 HG02148.hp2 |
LOW | chr16 | C | G | TogoVar |
| 70259148:splice 70259148:variant goto | c.1824G>Ap.Thr608Thr | 320336 | Likely_benign | AARS1:16 | SO:0001819 synonymous_variant |
MONDO:MONDO:0018993 MedGen:C0270914 Orphanet:64746|MedGen:CN169374|MONDO:MONDO:0013212 MedGen:C2750090 OMIM:613287 others(2): Show |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0010 | a0001c0010t0001 | a0001c0010t0001g0187 | NA18983.hp2 | LOW | chr16 | C | T | TogoVar |
| 70265046:splice 70265046:variant goto | c.1404C>Tp.Tyr468Tyr | 239030 | Benign/Likely_benign | AARS1:16 | SO:0001819 synonymous_variant |
MONDO:MONDO:0013212 MedGen:C2750090 OMIM:613287 Orphanet:228174|MeSH:D030342 MedGen:C0950123|MedGen:CN169374|MONDO:MONDO:0018993 others(9): Show |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0012 | a0001c0012t0001 | a0001c0012t0001g0316 | HG04204.hp1 | LOW | chr16 | G | A | TogoVar |
| 70262421:splice 70262421:variant goto | c.1596C>Ap.Thr532Thr | 320339 | Conflicting_classifications_of_pathogenicity | AARS1:16 | SO:0001819 synonymous_variant |
MeSH:D030342 MedGen:C0950123|MONDO:MONDO:0013212 MedGen:C2750090 OMIM:613287 Orphanet:228174 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0013 | a0001c0013t0001 | a0001c0013t0001g0086 | NA19057.hp2 | LOW | chr16 | G | T | TogoVar |
| 70253771:splice 70253771:variant goto | c.2550C>Tp.Asp850Asp | 2202488 | Likely_benign | AARS1:16 | SO:0001819 synonymous_variant |
MONDO:MONDO:0018993 MedGen:C0270914 Orphanet:64746 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0016 | a0001c0016t0001 | a0001c0016t0001g0097 | HG01943.hp2 | LOW | chr16 | G | A | TogoVar |
| 70269734:splice 70269734:variant goto | c.846A>Gp.Lys282Lys | 476744 | Likely_benign | AARS1:16 | SO:0001819 synonymous_variant |
MONDO:MONDO:0018993 MedGen:C0270914 Orphanet:64746 |
- | 1 | 1 | 1 | 1 | a0001 | a0001c0019 | a0001c0019t0001 | a0001c0019t0001g0206 | HG03669.hp1 | LOW | chr16 | T | C | TogoVar |
| CHR:POS | annotationhgvs_chgvs_p | disease trait-log10podds or beta | AHAPIDS ahapids
|
ACHAPIDS achapids
|
ACTHAPIDS acthapids
|
ACTGHAPIDS actghapids
|
haplotypeids haplotypeids
|
study | initial sample size/replication sample size | report genes | mapped gene | strongest snp risk allele | strand strand
|
impact | chr | ref | alt |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr16:70275334
|
c.479+1152C>T | Body mass index | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0002a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0161others(34): Show | HG00099.hp2 HG00140.hp2 HG01070.hp2 HG01071.hp2 HG01074.hp1 others(35): Show |
Leveraging Polygenic Functional Enrichment to Impr others(15): Show |
approximately 458,000 European ancestry individual others(2): Show |
AARS1 | rs12149660-? | - | MODIFIER | chr16 | G | A | |
|
chr16:70275334
|
c.479+1152C>T | Adult body size0.0162176 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0002a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0161others(34): Show | HG00099.hp2 HG00140.hp2 HG01070.hp2 HG01071.hp2 HG01074.hp1 others(35): Show |
Use of genetic variation to separate the effects o others(80): Show |
453,169 European ancestry individuals/ | AARS | AARS1 | rs12149660-G | - | MODIFIER | chr16 | G | A |
|
chr16:70282008
|
c.144+612A>G | Body mass index (MTAG)0.01848 | a0001a0002a0003a0005a0006others(3): Show | a0001c0001a0001c0002a0001c0007a0001c0013a0001c0016others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006a0001c0001t0007a0001c0001t0008others(13): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(191): Show | HG00280.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp1 HG00423.hp2 others(192): Show |
Pleiotropic genetic architecture and novel loci fo others(28): Show |
694,649 European ancestry individuals/ | AARS1 | rs775208-T | - | MODIFIER | chr16 | T | C | |
|
chr16:70251998
|
c.*723T>C | Body mass index0.016 | a0001a0002a0003a0005a0006others(3): Show | a0001c0001a0001c0002a0001c0007a0001c0013a0001c0016others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006a0001c0001t0007a0001c0001t0008others(13): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(192): Show | HG00280.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp1 HG00423.hp2 others(193): Show |
Genomics and phenomics of body mass index reveals others(26): Show |
1,122,049 European ancestry individuals/ | AARS1 | rs4985407-G | - | MODIFIER | chr16 | A | G | |
|
chr16:70275334
|
c.479+1152C>T | Leucine levels10.027 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0002a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0161others(34): Show | HG00099.hp2 HG00140.hp2 HG01070.hp2 HG01071.hp2 HG01074.hp1 others(35): Show |
A cross-platform approach identifies genetic regul others(37): Show |
86,351 Caucasian ancestry individuals/ | AARS1 | rs12149660-G | - | MODIFIER | chr16 | G | A | |
|
chr16:70275334
|
c.479+1152C>T | Isoleucine levels9.492 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0002a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0161others(34): Show | HG00099.hp2 HG00140.hp2 HG01070.hp2 HG01071.hp2 HG01074.hp1 others(35): Show |
A cross-platform approach identifies genetic regul others(37): Show |
86,404 Caucasian ancestry individuals/ | AARS1 | rs12149660-G | - | MODIFIER | chr16 | G | A | |
|
chr16:70275334
|
c.479+1152C>T | Valine levels9.484 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0002a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0161others(34): Show | HG00099.hp2 HG00140.hp2 HG01070.hp2 HG01071.hp2 HG01074.hp1 others(35): Show |
A cross-platform approach identifies genetic regul others(37): Show |
85,641 Caucasian ancestry individuals/ | AARS1 | rs12149660-G | - | MODIFIER | chr16 | G | A | |
|
chr16:70275334
|
c.479+1152C>T | Valine levels0.0907 | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0002a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0161others(34): Show | HG00099.hp2 HG00140.hp2 HG01070.hp2 HG01071.hp2 HG01074.hp1 others(35): Show |
Genome-wide characterization of circulating metabo others(15): Show |
4,435 East Asian ancestry individuals, 11,340 Sout others(68): Show |
AARS1 | rs12149660-A | - | MODIFIER | chr16 | G | A | |
|
chr16:70292952
|
c.-3553A>T |
Alanine--tRNA ligase, cytoplasmic level in Chronic kidney disease with hypertension and no diabetes others(73): Show |
a0001a0002a0005 | a0001c0002a0002c0004a0005c0009 | a0001c0002t0001a0001c0002t0003a0001c0002t0004a0002c0004t0001a0005c0009t0001 | a0001c0002t0001g0001a0001c0002t0001g0148a0001c0002t0001g0296a0001c0002t0003g0322a0001c0002t0003g0323others(28): Show | HG01433.hp2 HG02055.hp2 HG02109.hp1 HG02109.hp2 HG02258.hp2 others(29): Show |
Identification of 969 protein quantitative trait l others(85): Show |
466 African American individuals/ | DDX19B | rs11859191-A | - | MODIFIER | chr16 | T | A | |
|
chr16:70269677
|
c.903C>Tp.His301His | Body mass index | a0001a0006a0007a0009a0010 | a0001c0001a0001c0007a0001c0013a0001c0016a0006c0018others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006a0001c0001t0007a0001c0001t0008others(7): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(156): Show | HG00280.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp1 HG00423.hp2 others(156): Show |
Shared Genetic and Experimental Links between Obes others(53): Show |
457,822 European ancestry individuals/ | NR | AARS1 | rs2070203-? | - | LOW | chr16 | G | A |
|
chr16:70275334
|
c.479+1152C>T | Body mass index | a0001 | a0001c0002 | a0001c0002t0001 | a0001c0002t0001g0002a0001c0002t0001g0154a0001c0002t0001g0155a0001c0002t0001g0156a0001c0002t0001g0161others(34): Show | HG00099.hp2 HG00140.hp2 HG01070.hp2 HG01071.hp2 HG01074.hp1 others(35): Show |
Shared Genetic and Experimental Links between Obes others(53): Show |
457,822 European ancestry individuals/ | NR | AARS1 | rs12149660-? | - | MODIFIER | chr16 | G | A |
|
chr16:70282008
|
c.144+612A>G | Body mass index0.0171458 | a0001a0002a0003a0005a0006others(3): Show | a0001c0001a0001c0002a0001c0007a0001c0013a0001c0016others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006a0001c0001t0007a0001c0001t0008others(13): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(191): Show | HG00280.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp1 HG00423.hp2 others(192): Show |
Genetic evidence that high BMI in childhood has a others(146): Show |
441,761 European ancestry individuals/ | AARS1 | rs775208-T | - | MODIFIER | chr16 | T | C | |
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chr16:70282008
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c.144+612A>G | Body mass index0.016308 | a0001a0002a0003a0005a0006others(3): Show | a0001c0001a0001c0002a0001c0007a0001c0013a0001c0016others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006a0001c0001t0007a0001c0001t0008others(13): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(191): Show | HG00280.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp1 HG00423.hp2 others(192): Show |
New role of fat-free mass in cancer risk linked wi others(26): Show |
342,566 European ancestry individuals/ | AARS1 | rs775208-C | - | MODIFIER | chr16 | T | C | |
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chr16:70282008
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c.144+612A>G | Body mass index or knee osteoarthritis (pleiotropy)others(11): Show | a0001a0002a0003a0005a0006others(3): Show | a0001c0001a0001c0002a0001c0007a0001c0013a0001c0016others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006a0001c0001t0007a0001c0001t0008others(13): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(191): Show | HG00280.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp1 HG00423.hp2 others(192): Show |
A sex- and site-specific relationship between body others(81): Show |
806,834 European ancestry BMI individuals, 62,497 others(80): Show |
AARS1 | rs775208-T | - | MODIFIER | chr16 | T | C | |
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chr16:70282008
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c.144+612A>G | Weight0.0104 | a0001a0002a0003a0005a0006others(3): Show | a0001c0001a0001c0002a0001c0007a0001c0013a0001c0016others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0006a0001c0001t0007a0001c0001t0008others(13): Show | a0001c0001t0001g0003a0001c0001t0001g0006a0001c0001t0001g0007a0001c0001t0001g0008a0001c0001t0001g0010others(191): Show | HG00280.hp1 HG00280.hp2 HG00323.hp1 HG00423.hp1 HG00423.hp2 others(192): Show |
A cross-population atlas of genetic associations f others(24): Show |
360,116 European ancestry individuals, 165,419 Eas others(29): Show |
AARS1 | rs775208-C | - | MODIFIER | chr16 | T | C |