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rs4924935

From SNPedia

Orientationplus
Stabilizedplus
Make rs4924935(C;C)
Make rs4924935(C;T)
Make rs4924935(T;T)
ReferenceGRCh38 38.1/141
Chromosome17
Position18850557
GeneLOC101929141
is asnp
is mentioned by
dbSNPrs4924935
ebirs4924935
HLIrs4924935
Exacrs4924935
Varsomers4924935
Maprs4924935
PheGenIrs4924935
hapmaprs4924935
1000 genomesrs4924935
hgdprs4924935
ensemblrs4924935
gopubmedrs4924935
geneviewrs4924935
scholarrs4924935
googlers4924935
pharmgkbrs4924935
gwascentralrs4924935
openSNPrs4924935
23andMers4924935
23andMe allrs4924935
SNP Nexus

SNPshotrs4924935
SNPdbers4924935
MSV3drs4924935
GWAS Ctlgrs4924935
GMAF0.2176
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 1.37 [1.19-1.58]


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