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rs3819102

From SNPedia

Orientationminus
Stabilizedminus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs3819102(C;C)
Make rs3819102(C;T)
ReferenceGRCh37 37.1/131
Chromosome18
Position675307
GeneENOSF1
is asnp
is mentioned by
dbSNPrs3819102
ebirs3819102
HLIrs3819102
Exacrs3819102
Varsomers3819102
Maprs3819102
PheGenIrs3819102
hapmaprs3819102
1000 genomesrs3819102
hgdprs3819102
ensemblrs3819102
gopubmedrs3819102
geneviewrs3819102
scholarrs3819102
googlers3819102
pharmgkbrs3819102
gwascentralrs3819102
openSNPrs3819102
23andMers3819102
23andMe allrs3819102
SNP Nexus

SNPshotrs3819102
SNPdbers3819102
MSV3drs3819102
GWAS Ctlgrs3819102
GMAF0.0877
Max Magnitude0
? (C;C) (C;T) (T;T) 28
[PMID 19190136OA-icon.png] rs3819102 associated with risk of endometrial cancer. The odds ratio (95% confidence interval) for the CC genotype was 1.5 (1.0-2.2) compared with the TT genotype