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rs7136702

From SNPedia

Orientationplus
Stabilizedplus
Make rs7136702(C;C)
Make rs7136702(C;T)
Make rs7136702(T;T)
ReferenceGRCh38 38.1/141
Chromosome12
Position50486433
is asnp
is mentioned by
dbSNPrs7136702
ebirs7136702
HLIrs7136702
Exacrs7136702
Varsomers7136702
Maprs7136702
PheGenIrs7136702
hapmaprs7136702
1000 genomesrs7136702
hgdprs7136702
ensemblrs7136702
gopubmedrs7136702
geneviewrs7136702
scholarrs7136702
googlers7136702
pharmgkbrs7136702
gwascentralrs7136702
openSNPrs7136702
23andMers7136702
23andMe allrs7136702
SNP Nexus

SNPshotrs7136702
SNPdbers7136702
MSV3drs7136702
GWAS Ctlgrs7136702
GMAF0.4637
Max Magnitude
? (C;C) (C;T) (T;T) 28
[PMID 22076443OA-icon.png] Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13

[PMID 20972440] Meta-analysis of three genome-wide association studies identifies susceptibility loci for colorectal cancer at 1q41, 3q26.2, 12q13.13 and 20q13.33.


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