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rs6736997

From SNPedia

Orientationplus
Stabilizedplus
Make rs6736997(A;A)
Make rs6736997(A;C)
Make rs6736997(C;C)
ReferenceGRCh38 38.1/141
Chromosome2
Position234706553
is asnp
is mentioned by
dbSNPrs6736997
ebirs6736997
HLIrs6736997
Exacrs6736997
Varsomers6736997
Maprs6736997
PheGenIrs6736997
hapmaprs6736997
1000 genomesrs6736997
hgdprs6736997
ensemblrs6736997
gopubmedrs6736997
geneviewrs6736997
scholarrs6736997
googlers6736997
pharmgkbrs6736997
gwascentralrs6736997
openSNPrs6736997
23andMers6736997
23andMe allrs6736997
SNP Nexus

SNPshotrs6736997
SNPdbers6736997
MSV3drs6736997
GWAS Ctlgrs6736997
GMAF0.3076
Max Magnitude
? (A;A) (A;C) (C;C) 28
GWAS snp
PMID [PMID 20686608OA-icon.png]
Trait
Title Genome-wide association study of pancreatic cancer in Japanese population
Risk Allele A
P-val 0.000006
Odds Ratio 1.57 [1.29-1.91]