| geneid | 92 |
|---|---|
| ensemblid | ENSG00000121989.15 |
| hgncid | 173 |
| symbol | ACVR2A |
| name | activin A receptor type 2A |
| refseq_nuc | NM_001616.5 |
| refseq_prot | NP_001607.1 |
| ensembl_nuc | ENST00000241416.12 |
| ensembl_prot | ENSP00000241416.7 |
| mane_status | MANE Select |
| chr | chr2 |
| start | 147845029 |
| end | 147930822 |
| strand | + |
| ver | v1.2 |
| region | chr2:147845029-147930822 |
| region5000 | chr2:147840029-147935822 |
| regionname0 | ACVR2A_chr2_147845029_147930822 |
| regionname5000 | ACVR2A_chr2_147840029_147935822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr2:147930821
|
G | A | 0.0059 | splice_region_variant | LOW | HG02258.hp1 HG02630.hp1 |
a0001 | a0001c0001a0001c0002 | a0001c0001t0021a0001c0002t0024 | a0001c0001t0021g0012a0001c0002t0024g0148 | 2 | 338 | 0 | ACVR2A | ENSG00000121989.15 | transcript | ENST00000241416.12 | protein_coding | 11/11 | c.*3547G>A |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ACVR2A | 1/1 | a0001 | 513 | 336 | 72 | 64 | 144 | 14 | 40 | subcellular location copy fasta | chr2 | 147840029 | 147935822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ACVR2A | 1/1 | c0001 | 1542 | 195 | 48 | 30 | 83 | 8 | 24 | copy fasta | chr2 | 147840029 | 147935822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| ACVR2A | 1/1 | a0001c0001 | 195 | 48 | 30 | 83 | 8 | 24 | 1542 | copy fasta | chr2 | 147840029 | 147935822 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 147845207 | + | 1 | -0.9720 | -0.9544 | -0.8950 | 0.0770 | acceptor | a0001c0001 | HG02738.hp2 HG03654.hp2 NA19081.hp2 |
HG02717.hp2 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147896301 | + | 2 | 0.9982 | 0.9982 | 0.9978 | 0.0004 | donor | a0001c0001 | HG03491.hp1 HG03516.hp2 |
HG00408.hp1 NA18959.hp2 NA18974.hp1 NA19066.hp1 |
ACVR2A | chr2 | 147840029 | 147935822 |
| 147896508 | + | 2 | -0.9998 | -0.9997 | -0.9997 | 0.0000 | acceptor | a0001c0001 | HG00408.hp1 HG01243.hp2 HG02145.hp1 HG02630.hp2 HG02647.hp1 others(10): Show |
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp2 HG00408.hp2 others(175): Show |
ACVR2A | chr2 | 147840029 | 147935822 |
| 147899458 | + | 3 | 0.9823 | 0.9818 | 0.9813 | 0.0010 | donor | a0001c0001 | HG02809.hp2 | HG02647.hp2 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147899567 | + | 3 | -0.9760 | -0.9757 | -0.9752 | 0.0007 | acceptor | a0001c0001 | HG03688.hp1 | HG02647.hp2 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147899744 | + | 4 | 0.9899 | 0.9894 | 0.9886 | 0.0013 | donor | a0001c0001 | HG00642.hp2 | HG03688.hp1 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147899898 | + | 4 | -0.9836 | -0.9827 | -0.9817 | 0.0020 | acceptor | a0001c0001 | HG02922.hp1 | HG03688.hp1 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147915191 | + | 5 | 0.9944 | 0.9931 | 0.9926 | 0.0018 | donor | a0001c0001 | HG03453.hp1 HG03579.hp2 |
HG01168.hp1 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147915334 | + | 5 | -0.9924 | -0.9902 | -0.9899 | 0.0025 | acceptor | a0001c0001 | HG03453.hp1 HG03579.hp2 |
HG03654.hp2 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147917283 | + | 6 | 0.9996 | 0.9994 | 0.9994 | 0.0002 | donor | a0001c0001 | HG00408.hp1 NA18959.hp2 NA18974.hp1 NA19066.hp1 |
HG02145.hp1 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147917426 | + | 6 | -0.9998 | -0.9998 | -0.9998 | 0.0000 | acceptor | a0001c0001 | HG00408.hp1 NA18959.hp2 NA18974.hp1 NA19066.hp1 |
HG00099.hp1 HG00140.hp2 HG00280.hp2 HG00323.hp2 HG00408.hp2 others(181): Show |
ACVR2A | chr2 | 147840029 | 147935822 |
| 147918447 | + | 7 | 0.9974 | 0.9964 | 0.9950 | 0.0023 | donor | a0001c0001 | HG02071.hp1 | HG02145.hp1 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147918592 | + | 7 | -0.9949 | -0.9940 | -0.9938 | 0.0011 | acceptor | a0001c0001 | HG03516.hp2 | HG02071.hp1 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147920230 | + | 8 | 0.9945 | 0.9944 | 0.9938 | 0.0006 | donor | a0001c0001 | HG03831.hp2 | HG01167.hp1 HG02258.hp2 HG02486.hp1 HG03453.hp1 HG03579.hp2 |
ACVR2A | chr2 | 147840029 | 147935822 |
| 147920344 | + | 8 | -0.9973 | -0.9971 | -0.9969 | 0.0004 | acceptor | a0001c0001 | HG02071.hp2 HG02165.hp1 |
NA19087.hp1 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147922973 | + | 9 | 0.9888 | 0.9878 | 0.9872 | 0.0016 | donor | a0001c0001 | HG02738.hp2 | HG02683.hp1 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147923111 | + | 9 | -0.9853 | -0.9837 | -0.9820 | 0.0033 | acceptor | a0001c0001 | HG03471.hp2 | HG02683.hp1 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147926031 | + | 10 | 0.9992 | 0.9992 | 0.9992 | 0.0001 | donor | a0001c0001 | HG00738.hp2 HG01175.hp2 HG02015.hp2 HG02083.hp2 HG02155.hp1 others(36): Show |
HG03516.hp2 | ACVR2A | chr2 | 147840029 | 147935822 |
| 147926161 | + | 10 | -0.9979 | -0.9978 | -0.9977 | 0.0002 | acceptor | a0001c0001 | NA18612.hp2 | HG00639.hp1 HG00639.hp2 HG01167.hp1 HG01884.hp2 HG02055.hp2 others(20): Show |
ACVR2A | chr2 | 147840029 | 147935822 |
| 147927080 | + | 11 | 0.9855 | 0.9842 | 0.9837 | 0.0018 | donor | a0001c0001 | HG02965.hp2 | HG03516.hp2 | ACVR2A | chr2 | 147840029 | 147935822 |
| 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| 147935712:splice 147935712:variant goto | c.*8438G>T | 1634238 | Benign | ORC4:5000 | SO:0001627 intron_variant |
MedGen:C3661900 | + | 1 | 1 | 1 | 1 | a0001 | a0001c0001 | a0001c0001t0004 | a0001c0001t0004g0010 | HG02630.hp2 HG02647.hp1 |
MODIFIER | chr2 | G | T | 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 |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
|
chr2:147884240
|
c.56-12061T>C | Feeling hurt6.07 | a0001 | a0001c0001a0001c0003a0001c0004a0001c0008 | a0001c0001t0002a0001c0001t0004a0001c0001t0005a0001c0001t0008a0001c0001t0009others(9): Show | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0151a0001c0001t0002g0153a0001c0001t0002g0154others(111): Show | HG00140.hp2 HG00280.hp2 HG00323.hp2 HG00408.hp1 HG00408.hp2 others(115): Show |
Item-level analyses reveal genetic heterogeneity i others(14): Show |
372,047 European ancestry individuals/ | NR | ACVR2A | rs2113792-T | + | MODIFIER | chr2 | T | C |
|
chr2:147849869
|
c.55+4662G>A | Feeling tense5.46 | a0001 | a0001c0001 | a0001c0001t0002 | a0001c0001t0002g0207 | HG00323.hp2 |
Item-level analyses reveal genetic heterogeneity i others(14): Show |
371,318 European ancestry individuals/ | ACVR2A | ACVR2A | rs79861172-A | + | MODIFIER | chr2 | G | A |
|
chr2:147915821
|
c.672+487C>T | Neurociticism7.22 | a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0002a0001c0001t0005a0001c0001t0006a0001c0001t0009a0001c0001t0015others(8): Show | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0151a0001c0001t0002g0153a0001c0001t0002g0154others(102): Show | HG00140.hp2 HG00280.hp2 HG00323.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
Item-level analyses reveal genetic heterogeneity i others(14): Show |
380,506 European ancestry individuals/ | NR | ACVR2A | rs12622150-T | + | MODIFIER | chr2 | C | T |
|
chr2:147922691
|
c.1078-282G>A |
Glomerular filtration rate (creatinine)0 others(5): Show |
a0001a0002a0003 | a0001c0001a0001c0002a0001c0005a0001c0008a0002c0006others(1): Show | a0001c0001t0003a0001c0001t0007a0001c0001t0008a0001c0001t0016a0001c0001t0017others(16): Show | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(174): Show | HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
Genetic associations at 53 loci highlight cell typ others(56): Show |
133,413 European ancestry individuals/42,166 Europ others(108): Show |
ACVR2A | ACVR2A | rs3820716-A | + | MODIFIER | chr2 | G | A |
|
chr2:147861185
|
c.55+15978A>G | Neuroticism7.418 | a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0002a0001c0001t0005a0001c0001t0009a0001c0001t0015a0001c0001t0019others(5): Show | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0151a0001c0001t0002g0153a0001c0001t0002g0154others(99): Show | HG00140.hp2 HG00280.hp2 HG00323.hp2 HG00408.hp2 HG00438.hp1 others(102): Show |
Association analysis in over 329,000 individuals i others(59): Show |
329,821 European ancestry individuals/122,867 Euro others(25): Show |
intergenic | ACVR2A | rs7582403-A | + | MODIFIER | chr2 | A | G |
|
chr2:147930162
|
c.*2888A>C | Neuroticism6.073 | a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0016a0001c0001t0017 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(31): Show | HG00609.hp1 HG00673.hp1 HG00733.hp2 HG01081.hp1 HG01106.hp1 others(39): Show |
Meta-analysis of genome-wide association studies f others(81): Show |
449,484 European ancestry individuals/ | NR | ACVR2A | rs17692648-A | + | MODIFIER | chr2 | A | C |
|
chr2:147859811
|
c.55+14604C>G | Systolic blood pressure | a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0016a0001c0001t0017 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(31): Show | HG00609.hp1 HG00673.hp1 HG00733.hp2 HG01081.hp1 HG01106.hp1 others(39): Show |
Leveraging Polygenic Functional Enrichment to Impr others(15): Show |
approximately 422,000 European ancestry individual others(2): Show |
ACVR2A | rs17741978-? | + | MODIFIER | chr2 | C | G | |
|
chr2:147915821
|
c.672+487C>T | Neuroticism | a0001 | a0001c0001a0001c0003a0001c0004 | a0001c0001t0002a0001c0001t0005a0001c0001t0006a0001c0001t0009a0001c0001t0015others(8): Show | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0151a0001c0001t0002g0153a0001c0001t0002g0154others(102): Show | HG00140.hp2 HG00280.hp2 HG00323.hp2 HG00408.hp2 HG00438.hp1 others(105): Show |
Leveraging Polygenic Functional Enrichment to Impr others(15): Show |
approximately 372,000 European ancestry individual others(2): Show |
ACVR2A | rs12622150-? | + | MODIFIER | chr2 | C | T | |
|
chr2:147930355
|
c.*3081G>T | Eosinophil counts0.015255 | a0001 | a0001c0001 | a0001c0001t0022 | a0001c0001t0022g0163 | NA18989.hp2 |
Trans-ethnic and Ancestry-Specific Blood-Cell Gene others(54): Show |
474,237 European ancestry individuals/ | NR | ACVR2A | rs151062078-D | + | MODIFIER | chr2 | G | T |
|
chr2:147930355
|
c.*3098delT | Eosinophil counts0.015255 | a0001a0002a0003 | a0001c0001a0001c0002a0001c0005a0002c0006a0003c0007 | a0001c0001t0003a0001c0001t0004a0001c0001t0009a0001c0001t0016a0001c0002t0001others(11): Show | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(181): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
Trans-ethnic and Ancestry-Specific Blood-Cell Gene others(54): Show |
474,237 European ancestry individuals/ | NR | ACVR2A | rs151062078-D | + | MODIFIER | chr2 | GT | G |
|
chr2:147883199
|
c.56-13102T>C | Haemorrhoidal disease0.98 | a0001a0002a0003 | a0001c0001a0001c0002a0001c0005a0002c0006a0003c0007 | a0001c0001t0006a0001c0002t0001a0001c0002t0006a0001c0002t0010a0001c0002t0012others(10): Show | a0001c0001t0006g0094a0001c0002t0001g0004a0001c0002t0001g0005a0001c0002t0001g0006a0001c0002t0001g0008others(133): Show | HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00323.hp1 HG00423.hp1 others(134): Show |
Genome-wide analysis of 944 133 individuals provid others(55): Show |
218,920 European ancestry cases, 725,213 European others(18): Show |
ACVR2A | ACVR2A | rs7559714-? | + | MODIFIER | chr2 | T | C |
|
chr2:147930162
|
c.*2888A>C | Educational attainment | a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0016a0001c0001t0017 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(31): Show | HG00609.hp1 HG00673.hp1 HG00733.hp2 HG01081.hp1 HG01106.hp1 others(39): Show |
Genetic Risk for Smoking: Disentangling Interplay others(39): Show |
451,800 European or unknown ancestry individuals/ | ACVR2A | rs17692648-? | + | MODIFIER | chr2 | A | C | |
|
chr2:147930355
|
c.*3081G>T | Arterial stiffness index0.019 | a0001 | a0001c0001 | a0001c0001t0022 | a0001c0001t0022g0163 | NA18989.hp2 |
Genome-wide association study identifies loci for others(60): Show |
127,121 European ancestry individuals/ | ACVR2A | ACVR2A | rs151062078-? | + | MODIFIER | chr2 | G | T |
|
chr2:147930355
|
c.*3098delT | Arterial stiffness index0.019 | a0001a0002a0003 | a0001c0001a0001c0002a0001c0005a0002c0006a0003c0007 | a0001c0001t0003a0001c0001t0004a0001c0001t0009a0001c0001t0016a0001c0002t0001others(11): Show | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(181): Show | HG00099.hp1 HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00323.hp1 others(191): Show |
Genome-wide association study identifies loci for others(60): Show |
127,121 European ancestry individuals/ | ACVR2A | ACVR2A | rs151062078-? | + | MODIFIER | chr2 | GT | G |
|
chr2:147840650
|
c.-4503G>C | Gout1.046551 | a0001a0002a0003 | a0001c0001a0001c0002a0001c0005a0001c0008a0002c0006others(1): Show | a0001c0001t0003a0001c0001t0006a0001c0001t0007a0001c0001t0008a0001c0001t0017others(16): Show | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(174): Show | HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
A genome-wide association analysis reveals new pat others(25): Show |
77,627 European ancestry cases, 933,894 European a others(17): Show |
RNA5SP106 - ACVR2A | rs12989087-C | + | MODIFIER | chr2 | G | C | |
|
chr2:147840650
|
c.-4503G>C | Gout1.0320014 | a0001a0002a0003 | a0001c0001a0001c0002a0001c0005a0001c0008a0002c0006others(1): Show | a0001c0001t0003a0001c0001t0006a0001c0001t0007a0001c0001t0008a0001c0001t0017others(16): Show | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(174): Show | HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00323.hp1 HG00408.hp1 others(183): Show |
A genome-wide association analysis reveals new pat others(25): Show |
100,671 European ancestry cases, 2,106,212 Europea others(20): Show |
RNA5SP106 - ACVR2A | rs12989087-C | + | MODIFIER | chr2 | G | C | |
|
chr2:147876367
|
c.56-19934A>C |
Educational attainment (years of education) others(9): Show |
a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0016a0001c0001t0017 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(31): Show | HG00609.hp1 HG00673.hp1 HG00733.hp2 HG01081.hp1 HG01106.hp1 others(39): Show |
Gene discovery and polygenic prediction from a gen others(80): Show |
up to 1,131,881 European ancestry individuals/ | ACVR2A | rs17742342-A | + | MODIFIER | chr2 | A | C | |
|
chr2:147876367
|
c.56-19934A>C | Educational attainment (MTAG)0.0113 | a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0016a0001c0001t0017 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(31): Show | HG00609.hp1 HG00673.hp1 HG00733.hp2 HG01081.hp1 HG01106.hp1 others(39): Show |
Gene discovery and polygenic prediction from a gen others(80): Show |
1,311,438 European ancestry individuals/ | Intergenic | ACVR2A | rs17742342-A | + | MODIFIER | chr2 | A | C |
|
chr2:147869959
|
c.55+24752C>A | Urate levels0.0205 | a0001a0002a0003 | a0001c0001a0001c0002a0001c0005a0001c0008a0002c0006others(1): Show | a0001c0001t0006a0001c0001t0008a0001c0001t0028a0001c0002t0001a0001c0002t0006others(13): Show | a0001c0001t0006g0094a0001c0001t0008g0018a0001c0001t0008g0019a0001c0001t0008g0124a0001c0001t0008g0125others(139): Show | HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00323.hp1 HG00408.hp1 others(140): Show |
Urate, Blood Pressure, and Cardiovascular Disease: others(76): Show |
454,183 European ancestry individuals/ | NR | ACVR2A | rs929939-A | + | MODIFIER | chr2 | C | A |
|
chr2:147884240
|
c.56-12061T>C | Personality traits or cognitive traits (multivariate analysis)others(22): Show | a0001 | a0001c0001a0001c0003a0001c0004a0001c0008 | a0001c0001t0002a0001c0001t0004a0001c0001t0005a0001c0001t0008a0001c0001t0009others(9): Show | a0001c0001t0002g0009a0001c0001t0002g0013a0001c0001t0002g0151a0001c0001t0002g0153a0001c0001t0002g0154others(111): Show | HG00140.hp2 HG00280.hp2 HG00323.hp2 HG00408.hp1 HG00408.hp2 others(115): Show |
Multivariate genetic analysis of personality and c others(44): Show |
337,125 British ancestry individuals/ | ACVR2A | rs2113792-? | + | MODIFIER | chr2 | T | C | |
|
chr2:147879893
|
c.56-16408A>C | ICD10 M54: Dorsalgia0.96 | a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0016a0001c0001t0017 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(31): Show | HG00609.hp1 HG00673.hp1 HG00733.hp2 HG01081.hp1 HG01106.hp1 others(39): Show |
Rare SLC13A1 variants associate with intervertebra others(63): Show |
119,110 European ancestry cases, 909,847 European others(18): Show |
ACVR2A | rs7560502-C | + | MODIFIER | chr2 | A | C | |
|
chr2:147859811
|
c.55+14604C>G | Diastolic blood pressure0.1433 | a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0016a0001c0001t0017 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(31): Show | HG00609.hp1 HG00673.hp1 HG00733.hp2 HG01081.hp1 HG01106.hp1 others(39): Show |
Genome-wide analysis in over 1 million individuals others(86): Show |
1,028,980 European ancestry individuals/62,047 Afr others(62): Show |
ACVR2A | rs17741978-G | + | MODIFIER | chr2 | C | G | |
|
chr2:147930162
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c.*2888A>C | Height0.0131 | a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0016a0001c0001t0017 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(31): Show | HG00609.hp1 HG00673.hp1 HG00733.hp2 HG01081.hp1 HG01106.hp1 others(39): Show |
A saturated map of common genetic variants associa others(22): Show |
5,314,291 European ancestry, Hispanic or Latin Ame others(79): Show |
ACVR2A | rs17692648-C | + | MODIFIER | chr2 | A | C | |
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chr2:147876367
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c.56-19934A>C | Educational attainment0.0126672 | a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0016a0001c0001t0017 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(31): Show | HG00609.hp1 HG00673.hp1 HG00733.hp2 HG01081.hp1 HG01106.hp1 others(39): Show |
Polygenic prediction of educational attainment wit others(88): Show |
3,037,499 European ancestry individuals/ | ACVR2A | rs17742342-A | + | MODIFIER | chr2 | A | C | |
|
chr2:147859811
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c.55+14604C>G | Systolic blood pressure0.1742 | a0001 | a0001c0001 | a0001c0001t0003a0001c0001t0007a0001c0001t0016a0001c0001t0017 | a0001c0001t0003g0001a0001c0001t0003g0002a0001c0001t0003g0003a0001c0001t0003g0016a0001c0001t0003g0017others(31): Show | HG00609.hp1 HG00673.hp1 HG00733.hp2 HG01081.hp1 HG01106.hp1 others(39): Show |
Genome-wide analysis in over 1 million individuals others(86): Show |
1,028,980 European ancestry individuals/40,204 Afr others(62): Show |
ACVR2A | rs17741978-G | + | MODIFIER | chr2 | C | G | |
|
chr2:147873663
|
c.56-22638A>T | Serum uric acid levels0.016 | a0001a0002a0003 | a0001c0001a0001c0002a0001c0005a0001c0008a0002c0006others(1): Show | a0001c0001t0003a0001c0001t0006a0001c0001t0008a0001c0001t0028a0001c0002t0001others(14): Show | a0001c0001t0003g0194a0001c0001t0003g0292a0001c0001t0006g0094a0001c0001t0008g0018a0001c0001t0008g0019others(141): Show | HG00099.hp2 HG00140.hp1 HG00280.hp1 HG00323.hp1 HG00408.hp1 others(142): Show |
A cross-population atlas of genetic associations f others(24): Show |
343,836 European ancestry individuals, 129,405 Eas others(29): Show |
ACVR2A | rs13021972-T | + | MODIFIER | chr2 | A | T |