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rs10088262

From SNPedia

Orientationplus
Stabilizedplus
Make rs10088262(A;A)
Make rs10088262(A;G)
Make rs10088262(G;G)
ReferenceGRCh38 38.1/141
Chromosome8
Position123753462
is asnp
is mentioned by
dbSNPrs10088262
ebirs10088262
HLIrs10088262
Exacrs10088262
Varsomers10088262
Maprs10088262
PheGenIrs10088262
hapmaprs10088262
1000 genomesrs10088262
hgdprs10088262
ensemblrs10088262
gopubmedrs10088262
geneviewrs10088262
scholarrs10088262
googlers10088262
pharmgkbrs10088262
gwascentralrs10088262
openSNPrs10088262
23andMers10088262
23andMe allrs10088262
SNP Nexus

SNPshotrs10088262
SNPdbers10088262
MSV3drs10088262
GWAS Ctlgrs10088262
GMAF0.4504
Max Magnitude
? (A;A) (A;G) (G;G) 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 0.000004
Odds Ratio 1.40 [1.21-1.61]


[PMID 26304507] Association of gastrointestinal gland cancer susceptibility loci with esophageal carcinoma among the Chinese Han population: a case-control study