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rs10935838

From SNPedia

Orientationplus
Stabilizedplus
Make rs10935838(A;A)
Make rs10935838(A;G)
Make rs10935838(G;G)
ReferenceGRCh38 38.1/141
Chromosome3
Position151340459
GeneMED12L, P2RY12
is asnp
is mentioned by
dbSNPrs10935838
ebirs10935838
HLIrs10935838
Exacrs10935838
Varsomers10935838
Maprs10935838
PheGenIrs10935838
hapmaprs10935838
1000 genomesrs10935838
hgdprs10935838
ensemblrs10935838
gopubmedrs10935838
geneviewrs10935838
scholarrs10935838
googlers10935838
pharmgkbrs10935838
gwascentralrs10935838
openSNPrs10935838
23andMers10935838
23andMe allrs10935838
SNP Nexus

SNPshotrs10935838
SNPdbers10935838
MSV3drs10935838
GWAS Ctlgrs10935838
GMAF0.1515
Max Magnitude
[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)