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rs6691170

From SNPedia

Orientationplus
Stabilizedplus
Make rs6691170(G;G)
Make rs6691170(G;T)
Make rs6691170(T;T)
ReferenceGRCh38 38.1/141
Chromosome1
Position221872104
is asnp
is mentioned by
dbSNPrs6691170
ebirs6691170
HLIrs6691170
Exacrs6691170
Varsomers6691170
Maprs6691170
PheGenIrs6691170
hapmaprs6691170
1000 genomesrs6691170
hgdprs6691170
ensemblrs6691170
gopubmedrs6691170
geneviewrs6691170
scholarrs6691170
googlers6691170
pharmgkbrs6691170
gwascentralrs6691170
openSNPrs6691170
23andMers6691170
23andMe allrs6691170
SNP Nexus

SNPshotrs6691170
SNPdbers6691170
MSV3drs6691170
GWAS Ctlgrs6691170
GMAF0.2608
Max Magnitude
? (G;G) (G;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 T
P-val 1E-9
Odds Ratio 1.0600 [1.03-1.09]


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


[PMID 22629442OA-icon.png] Evaluation of Allele-Specific Somatic Changes of Genome-Wide Association Study Susceptibility Alleles in Human Colorectal Cancers


[PMID 22675446OA-icon.png] Colorectal Cancer Linkage on Chromosomes 4q21, 8q13, 12q24, and 15q22


[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.