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rs11255841

From SNPedia

Orientationplus
Stabilizedplus
Make rs11255841(A;A)
Make rs11255841(A;T)
Make rs11255841(T;T)
ReferenceGRCh38 38.1/142
Chromosome10
Position8697617
is asnp
is mentioned by
dbSNPrs11255841
dbSNP (classic)rs11255841
ClinGenrs11255841
ebirs11255841
HLIrs11255841
Exacrs11255841
Gnomadrs11255841
Varsomers11255841
LitVarrs11255841
Maprs11255841
PheGenIrs11255841
Biobankrs11255841
1000 genomesrs11255841
hgdprs11255841
ensemblrs11255841
geneviewrs11255841
scholarrs11255841
googlers11255841
pharmgkbrs11255841
gwascentralrs11255841
openSNPrs11255841
23andMers11255841
SNPshotrs11255841
SNPdbers11255841
MSV3drs11255841
GWAS Ctlgrs11255841
Max Magnitude0
GWAS snp
PMID [PMID 24737748OA-icon.png]
Trait Colorectal cancer
Title Identification of susceptibility loci for colorectal cancer in a genome-wide meta-analysis.
Risk Allele T
P-val 7E-11
Odds Ratio 1.19 [NR]


[PMID 33534415OA-icon.png] Familial Colorectal Cancer and Genetic Susceptibility: Colorectal Risk Variants in First-Degree Relatives of Patients With Colorectal Cancer.