| geneid | 9508 |
|---|---|
| ensemblid | ENSG00000156140.11 |
| hgncid | 219 |
| symbol | ADAMTS3 |
| name | ADAM metallopeptidase with thrombospondin type 1 motif 3 |
| refseq_nuc | NM_014243.3 |
| refseq_prot | NP_055058.2 |
| ensembl_nuc | ENST00000286657.10 |
| ensembl_prot | ENSP00000286657.4 |
| mane_status | MANE Select |
| chr | chr4 |
| start | 72280969 |
| end | 72569221 |
| strand | - |
| ver | v1.2 |
| region | chr4:72280969-72569221 |
| region5000 | chr4:72275969-72574221 |
| regionname0 | ADAMTS3_chr4_72280969_72569221 |
| regionname5000 | ADAMTS3_chr4_72275969_72574221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr4:72548569
|
C | T | 0.7528 | missense_variant | MODERATE | HG00140.hp2 HG00408.hp2 HG00609.hp2 others(134): Show |
a0001a0003a0004others(5): Show | a0001c0001a0001c0003a0001c0004others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003others(42): Show | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0075others(134): Show | 137 | 182 | 0 | ADAMTS3 | ENSG00000156140.11 | transcript | ENST00000286657.10 | protein_coding | 3/22 | c.413G>A | p.Arg138Lys | 872/6244 | 413/3618 | 138/1205 |
| 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 |
|---|
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr4:72281815
|
G | GA | 0.7802 | 3_prime_UTR_variant | MODIFIER | HG00140.hp1 HG00140.hp2 HG00408.hp1 others(139): Show |
a0001a0002a0006others(3): Show | a0001c0001a0001c0003a0001c0004others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0005others(31): Show | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0075others(139): Show | 142 | 182 | 1 | ADAMTS3 | ENSG00000156140.11 | transcript | ENST00000286657.10 | protein_coding | 22/22 | c.*1320dupT | 1320 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ADAMTS3 | 0/1 | a0001 | 1205 | 124 | 52 | 15 | 45 | 1 | 10 | subcellular location copy fasta | chr4 | 72275969 | 72574221 |
| 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
|
chapid | clen | total | AFR | AMR | EAS | EUR | SAS | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ADAMTS3 | 0/1 | c0001 | 3618 | 103 | 34 | 14 | 44 | 1 | 9 | copy fasta | chr4 | 72275969 | 72574221 |
| genename | grch38/chm13v2 | thapid | tlen | total | AFR | AMR | EAS | EUR | SAS | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ADAMTS3 | 0/1 | t0001 | 2628 | 83 | 29 | 18 | 24 | 1 | 10 | copy fasta | chr4 | 72275969 | 72574221 |
| 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 |
achapid | total | AFR | AMR | EAS | EUR | SAS | clen | cseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ADAMTS3 | 0/1 | a0001c0001 | 103 | 34 | 14 | 44 | 1 | 9 | 3618 | copy fasta | chr4 | 72275969 | 72574221 |
| 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 |
acthapid | total | AFR | AMR | EAS | EUR | SAS | tlen | tseq | chr | start | end |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ADAMTS3 | 0/1 | a0001c0001t0001 | 41 | 14 | 8 | 12 | 0 | 6 | 6245 | copy fasta | chr4 | 72275969 | 72574221 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72568694 | - | 1 | -0.5548 | -0.5088 | -0.4854 | 0.0695 | acceptor | a0001c0001t0001 | HG03516.hp1 NA19030.hp1 |
HG03490.hp1 HG03492.hp1 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72567374 | - | 2 | -0.7758 | -0.7640 | -0.7603 | 0.0154 | acceptor | a0001c0001t0001 | NA18992.hp1 | HG02572.hp2 HG03130.hp2 HG03540.hp2 NA18906.hp2 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72567401 | - | 2 | 0.8026 | 0.8010 | 0.6639 | 0.1388 | donor | a0001c0001t0001 | HG02602.hp1 | HG03490.hp1 HG03492.hp1 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72548478 | - | 3 | -0.9812 | -0.9648 | -0.9586 | 0.0225 | acceptor | a0001c0001t0001 | HG02165.hp1 | NA19030.hp2 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72548884 | - | 3 | 0.9958 | 0.9951 | 0.9939 | 0.0019 | donor | a0001c0001t0001 | HG02559.hp2 | HG01243.hp1 HG02258.hp1 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72414815 | - | 4 | -0.9838 | -0.9771 | -0.9770 | 0.0068 | acceptor | a0001c0001t0001 | NA19030.hp1 | HG01109.hp1 HG01433.hp1 HG02027.hp2 HG02080.hp1 HG03516.hp1 others(1): Show |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72414971 | - | 4 | 0.9994 | 0.9994 | 0.9993 | 0.0001 | donor | a0001c0001t0001 | HG01109.hp1 HG02027.hp2 HG02080.hp1 HG03516.hp1 NA18977.hp1 others(2): Show |
HG00609.hp2 HG01081.hp1 HG01243.hp1 HG02258.hp1 HG02572.hp2 others(7): Show |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72339494 | - | 5 | -0.9975 | -0.9973 | -0.9971 | 0.0004 | acceptor | a0001c0001t0001 | HG01167.hp1 | NA18939.hp1 NA18994.hp2 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72339693 | - | 5 | 0.9952 | 0.9947 | 0.9941 | 0.0010 | donor | a0001c0001t0001 | HG01243.hp1 | HG02258.hp1 HG02559.hp2 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72323014 | - | 6 | -0.8635 | -0.8493 | -0.8477 | 0.0158 | acceptor | a0001c0001t0001 | HG02572.hp2 HG03130.hp2 HG03540.hp2 NA18906.hp2 |
NA19030.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72323097 | - | 6 | 0.8433 | 0.8347 | 0.8272 | 0.0162 | donor | a0001c0001t0001 | NA18977.hp1 NA18992.hp1 |
HG02572.hp2 HG03130.hp2 HG03540.hp2 NA18906.hp2 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72320714 | - | 7 | -0.7120 | -0.6967 | -0.6406 | 0.0714 | acceptor | a0001c0001t0001 | NA18977.hp1 NA18992.hp1 |
HG02080.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72320870 | - | 7 | 0.7787 | 0.7742 | 0.7438 | 0.0349 | donor | a0001c0001t0001 | HG01243.hp1 | HG02080.hp1 NA18939.hp1 NA18994.hp2 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72319858 | - | 8 | -0.9128 | -0.9075 | -0.8954 | 0.0174 | acceptor | a0001c0001t0001 | HG01070.hp1 HG01081.hp2 HG01109.hp1 HG01167.hp1 HG01433.hp1 others(7): Show |
NA19030.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72319963 | - | 8 | 0.8774 | 0.8579 | 0.8521 | 0.0253 | donor | a0001c0001t0001 | NA18977.hp1 NA18992.hp1 |
NA19030.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72319332 | - | 9 | -0.9697 | -0.9602 | -0.9331 | 0.0366 | acceptor | a0001c0001t0001 | NA18977.hp1 NA18992.hp1 |
NA19030.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72319475 | - | 9 | 0.9494 | 0.9482 | 0.9362 | 0.0131 | donor | a0001c0001t0001 | NA19030.hp2 | NA18977.hp1 NA18992.hp1 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72318572 | - | 10 | -0.9972 | -0.9969 | -0.9968 | 0.0004 | acceptor | a0001c0001t0001 | HG02572.hp2 HG03540.hp2 NA18906.hp2 |
HG01243.hp1 NA18939.hp1 NA18994.hp2 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72318704 | - | 10 | 0.9968 | 0.9965 | 0.9962 | 0.0006 | donor | a0001c0001t0001 | HG02572.hp2 HG03540.hp2 NA18906.hp2 |
NA19030.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72315858 | - | 11 | -0.9993 | -0.9993 | -0.9993 | 0.0000 | acceptor | a0001c0001t0001 | HG01070.hp1 HG01081.hp2 HG01109.hp1 HG01167.hp1 HG01243.hp1 others(18): Show |
HG02451.hp2 NA18974.hp2 NA19030.hp2 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72315971 | - | 11 | 0.9968 | 0.9966 | 0.9964 | 0.0003 | donor | a0001c0001t0001 | NA19082.hp1 | NA19030.hp2 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72313677 | - | 12 | -0.9981 | -0.9980 | -0.9980 | 0.0001 | acceptor | a0001c0001t0001 | NA19030.hp1 | HG02572.hp2 HG03130.hp2 HG03540.hp2 NA18906.hp2 NA19043.hp1 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72313822 | - | 12 | 0.9969 | 0.9969 | 0.9968 | 0.0002 | donor | a0001c0001t0001 | NA19030.hp1 | HG02572.hp2 HG03130.hp2 HG03540.hp2 NA18906.hp2 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72312291 | - | 13 | -0.9967 | -0.9967 | -0.9966 | 0.0001 | acceptor | a0001c0001t0001 | NA19082.hp1 | NA19030.hp2 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72312466 | - | 13 | 0.9974 | 0.9972 | 0.9969 | 0.0004 | donor | a0001c0001t0001 | NA19030.hp1 | HG02572.hp2 HG03130.hp2 HG03540.hp2 NA18906.hp2 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72311048 | - | 14 | -0.9978 | -0.9978 | -0.9977 | 0.0002 | acceptor | a0001c0001t0001 | HG01070.hp1 HG01081.hp2 HG01109.hp1 HG01167.hp1 HG02080.hp1 others(7): Show |
HG02886.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72311181 | - | 14 | 0.9954 | 0.9953 | 0.9943 | 0.0011 | donor | a0001c0001t0001 | NA19082.hp1 | HG02572.hp2 HG03130.hp2 HG03540.hp2 NA18906.hp2 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72309397 | - | 15 | -0.9391 | -0.9370 | -0.9129 | 0.0262 | acceptor | a0001c0001t0001 | NA19082.hp1 | NA19030.hp2 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72309520 | - | 15 | 0.7756 | 0.7688 | 0.7511 | 0.0245 | donor | a0001c0001t0001 | NA19082.hp1 | HG02886.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72305987 | - | 16 | -0.9624 | -0.9612 | -0.9586 | 0.0038 | acceptor | a0001c0001t0001 | HG01109.hp1 HG01167.hp1 HG02257.hp2 homoSapiens_chm13v2.hp1 |
HG02886.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72306067 | - | 16 | 0.7905 | 0.7863 | 0.7797 | 0.0108 | donor | a0001c0001t0001 | HG03654.hp2 | HG02886.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72303917 | - | 17 | -0.9979 | -0.9971 | -0.9970 | 0.0008 | acceptor | a0001c0001t0001 | HG02886.hp1 | HG00609.hp2 HG01081.hp1 HG01243.hp1 HG01433.hp1 HG01496.hp2 others(12): Show |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72304080 | - | 17 | 0.9966 | 0.9948 | 0.9945 | 0.0021 | donor | a0001c0001t0001 | HG02886.hp1 | HG00609.hp2 HG01081.hp1 HG01243.hp1 HG01433.hp1 HG01496.hp2 others(11): Show |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72298277 | - | 18 | -0.8309 | -0.6462 | -0.6223 | 0.2085 | acceptor | a0001c0001t0001 | NA19030.hp2 | HG02027.hp2 HG03942.hp1 NA19030.hp1 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72298442 | - | 18 | 0.9095 | 0.7485 | 0.7221 | 0.1875 | donor | a0001c0001t0001 | NA19030.hp2 | HG03654.hp2 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72295654 | - | 19 | -0.9951 | -0.9945 | -0.9939 | 0.0012 | acceptor | a0001c0001t0001 | NA19030.hp2 | HG01081.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72295786 | - | 19 | 0.9950 | 0.9932 | 0.9931 | 0.0019 | donor | a0001c0001t0001 | NA19030.hp2 | HG02451.hp2 HG02886.hp1 |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72290855 | - | 20 | -0.9814 | -0.9799 | -0.9782 | 0.0032 | acceptor | a0001c0001t0001 | HG02165.hp1 | HG01070.hp1 HG01081.hp2 HG01109.hp1 HG02257.hp2 HG02602.hp1 others(2): Show |
ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72291062 | - | 20 | 0.9547 | 0.9496 | 0.9360 | 0.0187 | donor | a0001c0001t0001 | HG03516.hp1 | HG03490.hp2 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72288751 | - | 21 | -0.9968 | -0.9960 | -0.9953 | 0.0014 | acceptor | a0001c0001t0001 | HG01070.hp1 HG01081.hp2 HG01109.hp1 HG02257.hp2 HG02602.hp1 others(2): Show |
NA19030.hp2 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72288868 | - | 21 | 0.9979 | 0.9972 | 0.9960 | 0.0019 | donor | a0001c0001t0001 | NA19030.hp2 | HG01433.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 72283704 | - | 22 | 0.9795 | 0.9789 | 0.9754 | 0.0040 | donor | a0001c0001t0001 | HG01243.hp1 HG03041.hp2 |
HG02165.hp1 | ADAMTS3 | chr4 | 72275969 | 72574221 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 72548569:splice 72548569:variant goto | c.413G>Ap.Arg138Lys | 1189006 | Benign | ADAMTS3:9508 | SO:0001583 missense_variant |
MONDO:MONDO:0032564 MedGen:C4748408 OMIM:618154|MedGen:C3661900|. |
- | 8 | 17 | 45 | 137 | a0001a0003a0004a0005a0006others(3): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0011others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(40): Show | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083others(132): Show | HG00140.hp2 HG00408.hp2 HG00609.hp2 HG00639.hp1 HG00741.hp2 others(132): Show |
MODERATE | chr4 | C | T | TogoVar |
| 72309376:splice 72309376:variant goto | c.2179+21G>A | 1189005 | Benign | ADAMTS3:9508 | SO:0001627 intron_variant |
MONDO:MONDO:0032564 MedGen:C4748408 OMIM:618154|MedGen:C3661900 |
- | 9 | 20 | 51 | 177 | a0001a0002a0003a0004a0005others(4): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0011others(15): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(46): Show | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083others(172): Show | HG00140.hp1 HG00140.hp2 HG00408.hp1 HG00408.hp2 HG00609.hp1 others(172): Show |
MODIFIER | chr4 | C | T | TogoVar |
| 72414808:splice 72414808:variant goto | c.661+7G>A | 780467 | Benign/Likely_benign | ADAMTS3:9508 | SO:0001627 intron_variant |
MedGen:C3661900|.|MONDO:MONDO:0032564 MedGen:C4748408 OMIM:618154 |
- | 1 | 1 | 3 | 4 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0002a0001c0001t0005 | a0001c0001t0001g0073a0001c0001t0002g0019a0001c0001t0002g0020a0001c0001t0005g0010 | HG02486.hp1 NA19030.hp1 NA19240.hp1 NA20300.hp1 |
LOW | chr4 | C | T | TogoVar |
| 72568662:splice 72568662:variant goto | c.69+31delA | 1188859 | Benign | ADAMTS3:9508 | SO:0001627 intron_variant |
MONDO:MONDO:0032564 MedGen:C4748408 OMIM:618154 |
- | 8 | 16 | 49 | 165 | a0001a0002a0003a0004a0005others(3): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0015others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(44): Show | a0001c0001t0001g0089a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0099others(160): Show | HG00140.hp1 HG00140.hp2 HG00408.hp1 HG00408.hp2 HG00609.hp1 others(160): Show |
MODIFIER | chr4 | GT | G | TogoVar |
| 72567405:splice 72567405:variant goto | c.70-5delT | 3059242 | Benign | ADAMTS3:9508 | SO:0001627 intron_variant |
. | - | 6 | 9 | 29 | 79 | a0001a0002a0003a0004a0005others(1): Show | a0001c0001a0001c0003a0001c0004a0002c0002a0003c0007others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(24): Show | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0169others(74): Show | HG00140.hp2 HG00639.hp1 HG00741.hp2 HG01070.hp1 HG01081.hp2 others(74): Show |
LOW | chr4 | GA | G | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr4:72551807
|
c.98-2923C>T | Dental caries | a0001a0002a0003a0004a0005others(1): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0017others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0005a0001c0001t0010others(31): Show | a0001c0001t0001g0071a0001c0001t0001g0077a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(114): Show | HG00140.hp1 HG00140.hp2 HG00408.hp1 HG00609.hp1 HG00609.hp2 others(114): Show |
Genome-wide association scan of dental caries in t others(23): Show |
1,483 European ancestry comparatively younger indi others(65): Show |
ADAMTS3 | ADAMTS3 | rs1383934-? | - | MODIFIER | chr4 | G | A |
|
chr4:72551807
|
c.98-2923C>T | Dental caries | a0001a0002a0003a0004a0005others(1): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0017others(9): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0005a0001c0001t0010others(31): Show | a0001c0001t0001g0071a0001c0001t0001g0077a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093others(114): Show | HG00140.hp1 HG00140.hp2 HG00408.hp1 HG00609.hp1 HG00609.hp2 others(114): Show |
Genome-wide association scan of dental caries in t others(23): Show |
1,483 European ancestry comparatively younger indi others(65): Show |
ADAMTS3 | ADAMTS3 | rs1383934-? | - | MODIFIER | chr4 | G | A |
|
chr4:72499277
|
c.504+49201T>G |
Hip circumference adjusted for BMI0.0387 others(3): Show |
a0001a0002a0003a0008a0009 | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0011others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(32): Show | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0093others(132): Show | HG00140.hp1 HG00140.hp2 HG00408.hp1 HG00408.hp2 HG00609.hp1 others(132): Show |
GWAS of allometric body-shape indices in UK Bioban others(109): Show |
219,872 British ancestry women/ | ADAMTS3 | ADAMTS3 | rs788927-A | - | MODIFIER | chr4 | A | C |
|
chr4:72551305
|
c.98-2421C>T | Cortical surface area | a0001a0003a0004a0005a0006 | a0001c0001a0001c0003a0001c0004a0001c0017a0003c0007others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0005a0001c0001t0010others(17): Show | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0093a0001c0001t0001g0106others(53): Show | HG00140.hp2 HG00609.hp2 HG01081.hp1 HG01175.hp2 HG01243.hp1 others(53): Show |
Vertex-wise multivariate genome-wide association s others(76): Show |
35,657 White British ancestry individuals/ | NR | ADAMTS3 | rs67546436-A | - | MODIFIER | chr4 | G | A |
|
chr4:72508307
|
c.504+40171A>G | Cortical thickness | a0001a0002a0003a0004a0006others(1): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0017others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0005a0001c0001t0010others(21): Show | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0077a0001c0001t0001g0106a0001c0001t0001g0107others(62): Show | HG00140.hp2 HG00408.hp1 HG00609.hp2 HG01081.hp1 HG01175.hp2 others(62): Show |
Vertex-wise multivariate genome-wide association s others(76): Show |
35,657 White British ancestry individuals/ | NR | ADAMTS3 | rs788930-C | - | MODIFIER | chr4 | T | C |
|
chr4:72423246
|
c.505-8275G>A | Superior parietal area0.0407 | a0001a0002a0003a0006a0007others(2): Show | a0001c0001a0001c0003a0001c0011a0002c0002a0002c0009others(8): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(28): Show | a0001c0001t0001g0071a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0089others(105): Show | HG00140.hp1 HG00408.hp2 HG00609.hp1 HG00639.hp1 HG00639.hp2 others(105): Show |
Discovery of genomic loci of the human cerebral co others(46): Show |
32,488 European ancestry individuals/7,592 Europea others(58): Show |
ADAMTS3 | rs1871812-? | - | MODIFIER | chr4 | C | T | |
|
chr4:72496102
|
c.504+52376G>T | Height0.03169 | a0001a0002a0003a0008a0009 | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0011others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(32): Show | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0099others(131): Show | HG00140.hp1 HG00140.hp2 HG00408.hp1 HG00408.hp2 HG00609.hp1 others(131): Show |
A saturated map of common genetic variants associa others(22): Show |
293,593 African ancestry individuals/ | ADAMTS3 | rs700514-C | - | MODIFIER | chr4 | C | A | |
|
chr4:72520459
|
c.504+28019T>C | Height0.0109609 | a0001a0002a0003a0004a0005others(4): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0011others(14): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(43): Show | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083others(131): Show | HG00140.hp2 HG00408.hp1 HG00408.hp2 HG00609.hp2 HG00639.hp1 others(131): Show |
A Genomics England haplotype reference panel and i others(24): Show |
404,900 European ancestry individuals/ | ADAMTS3 | rs788940-? | - | MODIFIER | chr4 | A | G | |
|
chr4:72541929
|
c.504+6549A>T | Height0.033 | a0001a0002a0003a0007a0008others(1): Show | a0001c0001a0001c0003a0001c0004a0001c0011a0001c0012others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(20): Show | a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0093others(59): Show | HG00408.hp2 HG00639.hp1 HG00741.hp2 HG01070.hp1 HG01071.hp1 others(59): Show |
Your height affects your health: genetic determina others(42): Show |
67,452 Han Chinese ancestry individuals/ | ADAMTS3 | rs10027494-A | - | MODIFIER | chr4 | T | A | |
|
chr4:72470376
|
c.505-55405A>G | Vertex-wise cortical thickness8.03 | a0001a0002a0003 | a0001c0001a0001c0003a0001c0004a0002c0002a0003c0005 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0005a0001c0001t0010others(8): Show | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0146a0001c0001t0002g0034a0001c0001t0002g0037others(25): Show | HG00140.hp2 HG00408.hp1 HG00741.hp1 HG01081.hp1 HG01884.hp1 others(25): Show |
The genetic architecture of human cortical folding others(1): Show |
33,748 European ancestry individuals/ | ADAMTS3 | rs13128909-C | - | MODIFIER | chr4 | T | C | |
|
chr4:72470376
|
c.505-55409_505-55406delGTGT | Vertex-wise cortical thickness8.03 | a0001a0003a0006 | a0001c0001a0001c0003a0003c0008a0006c0016 | a0001c0001t0001a0001c0001t0002a0001c0001t0029a0001c0003t0001a0003c0008t0025others(1): Show | a0001c0001t0001g0091a0001c0001t0002g0027a0001c0001t0002g0030a0001c0001t0002g0032a0001c0001t0029g0160others(3): Show | HG01243.hp1 HG01243.hp2 HG01891.hp1 HG02451.hp1 HG02630.hp1 others(3): Show |
The genetic architecture of human cortical folding others(1): Show |
33,748 European ancestry individuals/ | ADAMTS3 | rs13128909-C | - | MODIFIER | chr4 | TACAC | T | |
|
chr4:72549013
|
c.98-129T>C | Vertex-wise cortical surface area9.24 | a0001a0003a0004a0006 | a0001c0001a0001c0003a0001c0004a0001c0017a0003c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0005a0001c0001t0010others(14): Show | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0106a0001c0001t0001g0107others(48): Show | HG00140.hp2 HG00609.hp2 HG01081.hp1 HG01175.hp2 HG01243.hp1 others(48): Show |
The genetic architecture of human cortical folding others(1): Show |
33,748 European ancestry individuals/ | ADAMTS3 | rs61317550-G | - | MODIFIER | chr4 | A | G | |
|
chr4:72451487
|
c.505-36516A>T | Vertex-wise sulcal depth11.68 | a0001a0002 | a0001c0001a0001c0004a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0005a0001c0001t0014others(5): Show | a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0146a0001c0001t0002g0034a0001c0001t0002g0037others(21): Show | HG00140.hp2 HG00408.hp1 HG00741.hp1 HG01081.hp1 HG01928.hp2 others(21): Show |
The genetic architecture of human cortical folding others(1): Show |
33,748 European ancestry individuals/ | ADAMTS3 | rs11932872-A | - | MODIFIER | chr4 | T | A | |
|
chr4:72554917
|
c.98-6033C>T | Coronary artery disease | a0001a0002a0008 | a0001c0001a0001c0015a0001c0017a0002c0002a0002c0020others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0013a0001c0001t0014a0001c0015t0009others(7): Show | a0001c0001t0001g0099a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(49): Show | HG00140.hp1 HG00408.hp1 HG00408.hp2 HG00609.hp1 HG00609.hp2 others(49): Show |
Discovery and systematic characterization of risk others(78): Show |
181,522 European ancestry, unknown cases, 984,168 others(36): Show |
ADAMTS3 | rs13105983-? | - | MODIFIER | chr4 | G | A | |
|
chr4:72520828
|
c.504+27650G>A | Height | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0013 | a0001c0001t0001g0099a0001c0001t0013g0004 | HG03834.hp2 HG03942.hp1 |
Leveraging Polygenic Functional Enrichment to Impr others(15): Show |
approximately 458,000 European ancestry individual others(2): Show |
ADAMTS3 | rs114506919-? | - | MODIFIER | chr4 | C | T | |
|
chr4:72554917
|
c.98-6033C>T | Coronary artery disease0.0293294 | a0001a0002a0008 | a0001c0001a0001c0015a0001c0017a0002c0002a0002c0020others(1): Show | a0001c0001t0001a0001c0001t0004a0001c0001t0013a0001c0001t0014a0001c0015t0009others(7): Show | a0001c0001t0001g0099a0001c0001t0001g0106a0001c0001t0001g0107a0001c0001t0001g0108a0001c0001t0001g0109others(49): Show | HG00140.hp1 HG00408.hp1 HG00408.hp2 HG00609.hp1 HG00609.hp2 others(49): Show |
Population-specific and trans-ancestry genome-wide others(85): Show |
25,892 Japanese ancestry cases, 95,342 European an others(85): Show |
ADAMTS3 | ADAMTS3 | rs13105983-? | - | MODIFIER | chr4 | G | A |
|
chr4:72549013
|
c.98-129T>C | Cortical surface area (MOSTest) | a0001a0003a0004a0006 | a0001c0001a0001c0003a0001c0004a0001c0017a0003c0007others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0005a0001c0001t0010others(14): Show | a0001c0001t0001g0071a0001c0001t0001g0091a0001c0001t0001g0092a0001c0001t0001g0106a0001c0001t0001g0107others(48): Show | HG00140.hp2 HG00609.hp2 HG01081.hp1 HG01175.hp2 HG01243.hp1 others(48): Show |
Understanding the genetic determinants of the brai others(15): Show |
26,502 European ancestry individuals/ | THADA, ZFP36L2, PLEKHH2 | ADAMTS3 | rs61317550-? | - | MODIFIER | chr4 | A | G |
|
chr4:72468334
|
c.505-53363C>A | Brain morphology (MOSTest) | a0001a0002a0003a0008a0009 | a0001c0001a0001c0003a0001c0011a0002c0002a0002c0009others(5): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(23): Show | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0093others(95): Show | HG00140.hp1 HG00408.hp2 HG00609.hp1 HG00639.hp1 HG00639.hp2 others(95): Show |
Understanding the genetic determinants of the brai others(15): Show |
26,502 European ancestry individuals/ | ADAMTS3 | ADAMTS3 | rs1383930-? | - | MODIFIER | chr4 | G | T |
|
chr4:72548569
|
c.413G>Ap.Arg138Lys | Diastolic blood pressure0.09444708 | a0001a0003a0004a0005a0006others(3): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0011others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(40): Show | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083others(132): Show | HG00140.hp2 HG00408.hp2 HG00609.hp2 HG00639.hp1 HG00741.hp2 others(132): Show |
Discovery of rare variants associated with blood p others(68): Show |
1,164,961 European ancestry individuals/ | ADAMTS3 | rs788908-T | - | MODERATE | chr4 | C | T | |
|
chr4:72548569
|
c.413G>Ap.Arg138Lys | Diastolic blood pressure0.0815 | a0001a0003a0004a0005a0006others(3): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0011others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(40): Show | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083others(132): Show | HG00140.hp2 HG00408.hp2 HG00609.hp2 HG00639.hp1 HG00741.hp2 others(132): Show |
Genome-wide analysis in over 1 million individuals others(86): Show |
1,028,980 European ancestry individuals/62,047 Afr others(62): Show |
ADAMTS3 | rs788908-T | - | MODERATE | chr4 | C | T | |
|
chr4:72522071
|
c.504+26407A>G | Height0.011 | a0001a0002a0003a0008 | a0001c0001a0001c0003a0001c0011a0001c0012a0002c0002others(3): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0007others(13): Show | a0001c0001t0001g0075a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0093a0001c0001t0001g0099others(47): Show | HG00408.hp2 HG00639.hp1 HG00741.hp2 HG01070.hp1 HG01071.hp1 others(47): Show |
A saturated map of common genetic variants associa others(22): Show |
5,314,291 European ancestry, Hispanic or Latin Ame others(79): Show |
ADAMTS3 | rs4694123-C | - | MODIFIER | chr4 | T | C | |
|
chr4:72478207
|
c.505-63236A>G | Waist circumference adjusted for body mass indexothers(17): Show | a0001a0002a0005 | a0001c0001a0001c0003a0001c0004a0001c0006a0002c0002others(2): Show | a0001c0001t0001a0001c0001t0019a0001c0001t0030a0001c0003t0001a0001c0003t0003others(5): Show | a0001c0001t0001g0071a0001c0001t0001g0092a0001c0001t0019g0033a0001c0001t0030g0181a0001c0003t0001g0090others(8): Show | HG02055.hp1 HG02258.hp1 HG02280.hp1 HG02630.hp2 HG02647.hp2 others(8): Show |
GWAS of allometric body-shape indices in UK Bioban others(109): Show |
219,872 British ancestry women/ | ADAMTS3 | ADAMTS3 | rs148537832-C | - | MODIFIER | chr4 | T | C |
|
chr4:72543951
|
c.504+4527G>A | Height0.0284 | a0001a0003a0004a0005a0006others(3): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0011others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(40): Show | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083others(132): Show | HG00140.hp2 HG00408.hp2 HG00609.hp2 HG00639.hp1 HG00741.hp2 others(132): Show |
A saturated map of common genetic variants associa others(22): Show |
472,730 East Asian ancestry individuals/ | ADAMTS3 | rs700513-C | - | MODIFIER | chr4 | C | T | |
|
chr4:72485105
|
c.504+63373C>T | Height0.0053 | a0001a0002 | a0001c0001a0002c0002a0002c0020 | a0001c0001t0001a0001c0001t0003a0002c0002t0001a0002c0002t0002a0002c0002t0003others(5): Show | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0003g0036a0002c0002t0001g0078a0002c0002t0001g0079others(33): Show | HG00140.hp1 HG00609.hp1 HG00639.hp2 HG01070.hp2 HG01071.hp2 others(33): Show |
A saturated map of common genetic variants associa others(22): Show |
5,314,291 European ancestry, Hispanic or Latin Ame others(79): Show |
ADAMTS3 | rs2086530-A | - | MODIFIER | chr4 | G | A | |
|
chr4:72563921
|
c.97+3453A>G | Height0.03 | a0001a0002a0003a0004a0005others(1): Show | a0001c0001a0001c0003a0001c0004a0002c0002a0003c0007others(4): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(25): Show | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0169others(75): Show | HG00140.hp2 HG00639.hp1 HG00741.hp2 HG01070.hp1 HG01081.hp2 others(75): Show |
A saturated map of common genetic variants associa others(22): Show |
5,314,291 European ancestry, Hispanic or Latin Ame others(79): Show |
ADAMTS3 | rs1518489-C | - | MODIFIER | chr4 | T | C | |
|
chr4:72571594
|
c.-2832C>A | Height0.0193 | a0001 | a0001c0001 | a0001c0001t0001a0001c0001t0004a0001c0001t0011 | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0169others(7): Show | HG00741.hp2 HG01070.hp1 HG01081.hp2 HG01109.hp1 HG01167.hp1 others(7): Show |
A saturated map of common genetic variants associa others(22): Show |
5,314,291 European ancestry, Hispanic or Latin Ame others(79): Show |
ADAMTS3 - HNRNPA1P67 | rs9884972-T | - | MODIFIER | chr4 | G | T | |
|
chr4:72393369
|
c.661+21446G>A | Vitamin D levels or COVID-19 (MTAG) | a0001a0002a0003a0004a0005others(2): Show | a0001c0001a0001c0003a0001c0004a0001c0011a0001c0012others(11): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(40): Show | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083others(153): Show | HG00140.hp1 HG00140.hp2 HG00408.hp1 HG00408.hp2 HG00609.hp1 others(153): Show |
Genetic correlation, causal relationship, and shar others(75): Show |
417,580 European ancestry individuals with vitamin others(95): Show |
ADAMTS3 | rs7686749-? | - | MODIFIER | chr4 | C | T | |
|
chr4:72513295
|
c.504+35183G>A |
Hip circumference adjusted for BMI0.0180 others(3): Show |
a0001a0002a0003a0004a0005others(4): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0011others(13): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(41): Show | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083others(128): Show | HG00140.hp2 HG00408.hp1 HG00408.hp2 HG00609.hp2 HG00639.hp1 others(128): Show |
GWAS of allometric body-shape indices in UK Bioban others(109): Show |
186,825 British ancestry men/ | ADAMTS3 | ADAMTS3 | rs788935-C | - | MODIFIER | chr4 | C | T |
|
chr4:72389836
|
c.661+24979G>A | Oral microbiome beta diversity (Euclidian distance) in oral squamous cell carcinomaothers(43): Show | a0001a0002 | a0001c0001a0001c0003a0002c0002 | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0016a0001c0001t0017others(6): Show | a0001c0001t0001g0071a0001c0001t0001g0089a0001c0001t0002g0052a0001c0001t0002g0063a0001c0001t0002g0066others(14): Show | HG01175.hp2 HG01884.hp2 HG02004.hp2 HG02165.hp2 HG02723.hp1 others(14): Show |
Host Genetic Associations with Salivary Microbiome others(16): Show |
144 individuals/ | ADAMTS3 | rs78182001-? | - | MODIFIER | chr4 | C | T | |
|
chr4:72450462
|
c.505-35491A>G | Height0.0188 | a0001a0002 | a0001c0001a0002c0002a0002c0020 | a0001c0001t0001a0001c0001t0003a0002c0002t0001a0002c0002t0002a0002c0002t0003others(5): Show | a0001c0001t0001g0113a0001c0001t0001g0114a0001c0001t0003g0036a0002c0002t0001g0078a0002c0002t0001g0079others(33): Show | HG00140.hp1 HG00609.hp1 HG00639.hp2 HG01070.hp2 HG01071.hp2 others(33): Show |
A saturated map of common genetic variants associa others(22): Show |
455,180 Hispanic or Latin American individuals/ | ADAMTS3 | rs11723034-C | - | MODIFIER | chr4 | T | C | |
|
chr4:72487704
|
c.504+60774C>A | Afamin levels1.07847 | a0001 | a0001c0001 | a0001c0001t0001 | a0001c0001t0001g0167 | HG01433.hp1 |
Differences and commonalities in the genetic archi others(76): Show |
2,935 Qatari ancestry individuals/ | ADAMTS3 | rs191962891-T | - | MODIFIER | chr4 | G | T | |
|
chr4:72474895
|
c.505-59924G>A | Brain morphology (MOSTest) | a0001a0002a0003a0007a0008others(1): Show | a0001c0001a0001c0003a0001c0011a0001c0012a0002c0002others(7): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(28): Show | a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083a0001c0001t0001g0089a0001c0001t0001g0093others(100): Show | HG00140.hp1 HG00408.hp2 HG00609.hp1 HG00639.hp1 HG00639.hp2 others(100): Show |
Boosting Schizophrenia Genetics by Utilizing Genet others(33): Show |
33,735 white British ancestry individuals/ | ADAMTS3 | rs11943308-? | - | MODIFIER | chr4 | C | T | |
|
chr4:72570878
|
c.-2116A>C | Multi-trait sex score | a0001a0002a0003a0004a0005others(2): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0002c0002others(6): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(22): Show | a0001c0001t0001g0163a0001c0001t0001g0164a0001c0001t0001g0166a0001c0001t0001g0167a0001c0001t0001g0169others(74): Show | HG00140.hp2 HG00639.hp1 HG00741.hp2 HG01070.hp1 HG01081.hp2 others(74): Show |
The genetics of a "femaleness/maleness" score in c others(40): Show |
141,980 European ancestry males/ | ADAMTS3 - HNRNPA1P67 | rs6834847-? | - | MODIFIER | chr4 | T | G | |
|
chr4:72548569
|
c.413G>Ap.Arg138Lys | Diastolic blood pressure0.10391903 | a0001a0003a0004a0005a0006others(3): Show | a0001c0001a0001c0003a0001c0004a0001c0006a0001c0011others(12): Show | a0001c0001t0001a0001c0001t0002a0001c0001t0003a0001c0001t0004a0001c0001t0005others(40): Show | a0001c0001t0001g0071a0001c0001t0001g0073a0001c0001t0001g0075a0001c0001t0001g0077a0001c0001t0001g0083others(132): Show | HG00140.hp2 HG00408.hp2 HG00609.hp2 HG00639.hp1 HG00741.hp2 others(132): Show |
Discovery of rare variants associated with blood p others(68): Show |
810,865 European ancestry individuals/ | ADAMTS3 | rs788908-T | - | MODERATE | chr4 | C | T |