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rs6879627

From SNPedia

Orientationplus
Stabilizedplus
Make rs6879627(C;C)
Make rs6879627(C;T)
Make rs6879627(T;T)
ReferenceGRCh38 38.1/141
Chromosome5
Position2109787
is asnp
is mentioned by
dbSNPrs6879627
ebirs6879627
HLIrs6879627
Exacrs6879627
Varsomers6879627
Maprs6879627
PheGenIrs6879627
hapmaprs6879627
1000 genomesrs6879627
hgdprs6879627
ensemblrs6879627
gopubmedrs6879627
geneviewrs6879627
scholarrs6879627
googlers6879627
pharmgkbrs6879627
gwascentralrs6879627
openSNPrs6879627
23andMers6879627
23andMe allrs6879627
SNP Nexus

SNPshotrs6879627
SNPdbers6879627
MSV3drs6879627
GWAS Ctlgrs6879627
GMAF0.2071
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 G
P-val 0.000008
Odds Ratio 1.25 [1.14-1.39]