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rs4822983

From SNPedia

Orientationplus
Stabilizedplus
Make rs4822983(C;C)
Make rs4822983(C;T)
Make rs4822983(T;T)
ReferenceGRCh38 38.1/141
Chromosome22
Position28719078
GeneCHEK2
is asnp
is mentioned by
dbSNPrs4822983
ebirs4822983
HLIrs4822983
Exacrs4822983
Varsomers4822983
Maprs4822983
PheGenIrs4822983
hapmaprs4822983
1000 genomesrs4822983
hgdprs4822983
ensemblrs4822983
gopubmedrs4822983
geneviewrs4822983
scholarrs4822983
googlers4822983
pharmgkbrs4822983
gwascentralrs4822983
openSNPrs4822983
23andMers4822983
23andMe allrs4822983
SNP Nexus

SNPshotrs4822983
SNPdbers4822983
MSV3drs4822983
GWAS Ctlgrs4822983
GMAF0.3072
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 22960999OA-icon.png]
Trait Esophageal cancer (squamous cell)
Title Genome-wide association analyses of esophageal squamous cell carcinoma in Chinese identify multiple susceptibility loci and gene-environment interactions.
Risk Allele T
P-val 2E-22
Odds Ratio 1.27 [1.21-1.34]