Have questions? Visit https://www.reddit.com/r/SNPedia

rs11169552

From SNPedia

Orientationplus
Stabilizedplus
Make rs11169552(C;C)
Make rs11169552(C;T)
Make rs11169552(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position50761880
is asnp
is mentioned by
dbSNPrs11169552
ebirs11169552
HLIrs11169552
Exacrs11169552
Varsomers11169552
Maprs11169552
PheGenIrs11169552
hapmaprs11169552
1000 genomesrs11169552
hgdprs11169552
ensemblrs11169552
gopubmedrs11169552
geneviewrs11169552
scholarrs11169552
googlers11169552
pharmgkbrs11169552
gwascentralrs11169552
openSNPrs11169552
23andMers11169552
23andMe allrs11169552
SNP Nexus

SNPshotrs11169552
SNPdbers11169552
MSV3drs11169552
GWAS Ctlgrs11169552
GMAF0.2369
Max Magnitude
? (C;C) (C;T) (T;T) 28
GWAS snp
PMID [PMID 20972440]
Trait
Title Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33
Risk Allele C
P-val 2E-10
Odds Ratio 1.0900 [1.05-1.11]


[PMID 22076443OA-icon.png] Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13


[PMID 22045029] Relationship between 16 susceptibility loci and colorectal cancer phenotype in 3146 patients.


[PMID 22999960OA-icon.png] Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.