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rs3917639

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(G;G) 0 common in complete genomics
Make rs3917639(A;A)
Make rs3917639(A;G)
ReferenceGRCh38 38.1/141
Chromosome1
Position94527220
GeneF3
is asnp
is mentioned by
dbSNPrs3917639
ebirs3917639
HLIrs3917639
Exacrs3917639
Varsomers3917639
Maprs3917639
PheGenIrs3917639
hapmaprs3917639
1000 genomesrs3917639
hgdprs3917639
ensemblrs3917639
gopubmedrs3917639
geneviewrs3917639
scholarrs3917639
googlers3917639
pharmgkbrs3917639
gwascentralrs3917639
openSNPrs3917639
23andMers3917639
23andMe allrs3917639
SNP Nexus

SNPshotrs3917639
SNPdbers3917639
MSV3drs3917639
GWAS Ctlgrs3917639
Max Magnitude0

[PMID 19583819] Tissue factor gene polymorphisms and haplotypes and the risk of ischemic vascular events: four studies and a meta-analysis