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rs2128382

From SNPedia

Orientationplus
Stabilizedplus
Make rs2128382(C;C)
Make rs2128382(C;T)
Make rs2128382(T;T)
ReferenceGRCh38 38.1/141
Chromosome8
Position129807793
is asnp
is mentioned by
dbSNPrs2128382
ebirs2128382
HLIrs2128382
Exacrs2128382
Varsomers2128382
Maprs2128382
PheGenIrs2128382
hapmaprs2128382
1000 genomesrs2128382
hgdprs2128382
ensemblrs2128382
gopubmedrs2128382
geneviewrs2128382
scholarrs2128382
googlers2128382
pharmgkbrs2128382
gwascentralrs2128382
openSNPrs2128382
23andMers2128382
23andMe allrs2128382
SNP Nexus

SNPshotrs2128382
SNPdbers2128382
MSV3drs2128382
GWAS Ctlgrs2128382
GMAF0.1299
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 23266556OA-icon.png]
Trait Colorectal cancer
Title Identification of Genetic Susceptibility Loci for Colorectal Tumors in a Genome-wide Meta-analysis.
Risk Allele
P-val 8E-6
Odds Ratio 1.11 [1.06-1.16]