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rs673604

From SNPedia

Orientationplus
Stabilizedplus
Geno Mag Summary
(T;T) 0 common in complete genomics
Make rs673604(C;C)
Make rs673604(C;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position35222214
is asnp
is mentioned by
dbSNPrs673604
ebirs673604
HLIrs673604
Exacrs673604
Varsomers673604
Maprs673604
PheGenIrs673604
hapmaprs673604
1000 genomesrs673604
hgdprs673604
ensemblrs673604
gopubmedrs673604
geneviewrs673604
scholarrs673604
googlers673604
pharmgkbrs673604
gwascentralrs673604
openSNPrs673604
23andMers673604
23andMe allrs673604
SNP Nexus

SNPshotrs673604
SNPdbers673604
MSV3drs673604
GWAS Ctlgrs673604
GMAF0.3985
Max Magnitude0
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 21499250OA-icon.png]
Trait
Title Genome-wide association study identifies a common variant associated with risk of endometrial cancer.
Risk Allele
P-val 0.000006
Odds Ratio 1.2100 [1.12-1.32]