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rs12615966

From SNPedia

Orientationplus
Stabilizedplus
Make rs12615966(C;C)
Make rs12615966(C;T)
Make rs12615966(T;T)
ReferenceGRCh38 38.1/141
Chromosome2
Position104762499
is asnp
is mentioned by
dbSNPrs12615966
ebirs12615966
HLIrs12615966
Exacrs12615966
Varsomers12615966
Maprs12615966
PheGenIrs12615966
hapmaprs12615966
1000 genomesrs12615966
hgdprs12615966
ensemblrs12615966
gopubmedrs12615966
geneviewrs12615966
scholarrs12615966
googlers12615966
pharmgkbrs12615966
gwascentralrs12615966
openSNPrs12615966
23andMers12615966
23andMe allrs12615966
SNP Nexus

SNPshotrs12615966
SNPdbers12615966
MSV3drs12615966
GWAS Ctlgrs12615966
GMAF0.1309
Max Magnitude
? (C;C) (C;T) (T;T) 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 0.000007
Odds Ratio 3.15 [1.91-5.21]