rs7163702
From SNPedia
| Orientation | minus |
| Stabilized | minus |
| Geno | Mag | Summary |
|---|---|---|
| (G;T) | 0 | common in complete genomics |
| Make rs7163702(G;G) |
| Make rs7163702(T;T) |
| Reference | GRCh37.p5 37.3/135 |
| Chromosome | 15 |
| Position | 28460135 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7163702 |
| dbSNP (classic) | rs7163702 |
| ClinGen | rs7163702 |
| ebi | rs7163702 |
| HLI | rs7163702 |
| Exac | rs7163702 |
| Gnomad | rs7163702 |
| Varsome | rs7163702 |
| LitVar | rs7163702 |
| Map | rs7163702 |
| PheGenI | rs7163702 |
| Biobank | rs7163702 |
| 1000 genomes | rs7163702 |
| hgdp | rs7163702 |
| ensembl | rs7163702 |
| geneview | rs7163702 |
| scholar | rs7163702 |
| rs7163702 | |
| pharmgkb | rs7163702 |
| gwascentral | rs7163702 |
| openSNP | rs7163702 |
| 23andMe | rs7163702 |
| SNPshot | rs7163702 |
| SNPdbe | rs7163702 |
| MSV3d | rs7163702 |
| GWAS Ctlg | rs7163702 |
| Max Magnitude | 0 |
[PMID 22076443
] Refinement of the associations between risk of colorectal cancer and polymorphisms on chromosomes 1q41 and 12q13.13
| ? | (G;G) (G;T) (T;T) | |
|---|---|---|
|
| ||
