rs7136702
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7136702(C;C) |
| Make rs7136702(C;T) |
| Make rs7136702(T;T) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 12 |
| Position | 50486433 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7136702 |
| dbSNP (classic) | rs7136702 |
| ClinGen | rs7136702 |
| ebi | rs7136702 |
| HLI | rs7136702 |
| Exac | rs7136702 |
| Gnomad | rs7136702 |
| Varsome | rs7136702 |
| LitVar | rs7136702 |
| Map | rs7136702 |
| PheGenI | rs7136702 |
| Biobank | rs7136702 |
| 1000 genomes | rs7136702 |
| hgdp | rs7136702 |
| ensembl | rs7136702 |
| geneview | rs7136702 |
| scholar | rs7136702 |
| rs7136702 | |
| pharmgkb | rs7136702 |
| gwascentral | rs7136702 |
| openSNP | rs7136702 |
| 23andMe | rs7136702 |
| SNPshot | rs7136702 |
| SNPdbe | rs7136702 |
| MSV3d | rs7136702 |
| GWAS Ctlg | rs7136702 |
| GMAF | 0.4637 |
| Max Magnitude | 0 |
| ? | (C;C) (C;T) (T;T) | 28 |
|---|---|---|
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[PMID 22076443
] 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 22999960] Much of the genetic risk of colorectal cancer is likely to be mediated through susceptibility to adenomas.
