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rs5853517

From SNPedia

Orientationplus
Stabilizedplus
Make rs5853517(-;-)
Make rs5853517(-;T)
Make rs5853517(T;T)
ReferenceGRCh38 38.1/141
Chromosome3
Position151339797
GeneMED12L, P2RY12
is asnp
is mentioned by
dbSNPrs5853517
ebirs5853517
HLIrs5853517
Exacrs5853517
Varsomers5853517
Maprs5853517
PheGenIrs5853517
hapmaprs5853517
1000 genomesrs5853517
hgdprs5853517
ensemblrs5853517
gopubmedrs5853517
geneviewrs5853517
scholarrs5853517
googlers5853517
pharmgkbrs5853517
gwascentralrs5853517
openSNPrs5853517
23andMers5853517
23andMe allrs5853517
SNP Nexus

SNPshotrs5853517
SNPdbers5853517
MSV3drs5853517
GWAS Ctlgrs5853517
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)