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rs5934683

From SNPedia

Orientationplus
Stabilizedplus
Make rs5934683(C;C)
Make rs5934683(C;T)
Make rs5934683(T;T)
ReferenceGRCh38 38.1/141
ChromosomeX
Position9783434
is asnp
is mentioned by
dbSNPrs5934683
ebirs5934683
HLIrs5934683
Exacrs5934683
Varsomers5934683
Maprs5934683
PheGenIrs5934683
hapmaprs5934683
1000 genomesrs5934683
hgdprs5934683
ensemblrs5934683
gopubmedrs5934683
geneviewrs5934683
scholarrs5934683
googlers5934683
pharmgkbrs5934683
gwascentralrs5934683
openSNPrs5934683
23andMers5934683
23andMe allrs5934683
SNP Nexus

SNPshotrs5934683
SNPdbers5934683
MSV3drs5934683
GWAS Ctlgrs5934683
GMAF0.3736
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22634755]
Trait
Title Common variation near CDKN1A, POLD3 and SHROOM2 influences colorectal cancer risk.
Risk Allele
P-val 7E-10
Odds Ratio 1.0700 None