rs10935838
From SNPedia
Orientation | plus |
Stabilized | plus |
Make rs10935838(A;A) |
Make rs10935838(A;G) |
Make rs10935838(G;G) |
Reference | GRCh38 38.1/141 |
Chromosome | 3 |
Position | 151340459 |
Gene | MED12L, P2RY12 |
is a | snp |
is | mentioned by |
dbSNP | rs10935838 |
dbSNP (classic) | rs10935838 |
ClinGen | rs10935838 |
ebi | rs10935838 |
HLI | rs10935838 |
Exac | rs10935838 |
Gnomad | rs10935838 |
Varsome | rs10935838 |
LitVar | rs10935838 |
Map | rs10935838 |
PheGenI | rs10935838 |
Biobank | rs10935838 |
1000 genomes | rs10935838 |
hgdp | rs10935838 |
ensembl | rs10935838 |
geneview | rs10935838 |
scholar | rs10935838 |
rs10935838 | |
pharmgkb | rs10935838 |
gwascentral | rs10935838 |
openSNP | rs10935838 |
23andMe | rs10935838 |
SNPshot | rs10935838 |
SNPdbe | rs10935838 |
MSV3d | rs10935838 |
GWAS Ctlg | rs10935838 |
GMAF | 0.1515 |
Max Magnitude | 0 |
[PMID 17707382] rs10935838, rs2046934, rs5853517, and rs6809699 venous thromboembolism lower risk of incident DVT/PE as compared to the reference haplotype H1 (odds ratio=0.50, 95% CI=0.27-0.93, p=0.028)