rs7797466
From SNPedia
| Orientation | plus |
| Stabilized | plus |
| Make rs7797466(A;A) |
| Make rs7797466(A;G) |
| Make rs7797466(G;G) |
| Reference | GRCh38 38.1/141 |
| Chromosome | 7 |
| Position | 6007152 |
| Gene | PMS2 |
| is a | snp |
| is | mentioned by |
| dbSNP | rs7797466 |
| dbSNP (classic) | rs7797466 |
| ClinGen | rs7797466 |
| ebi | rs7797466 |
| HLI | rs7797466 |
| Exac | rs7797466 |
| Gnomad | rs7797466 |
| Varsome | rs7797466 |
| LitVar | rs7797466 |
| Map | rs7797466 |
| PheGenI | rs7797466 |
| Biobank | rs7797466 |
| 1000 genomes | rs7797466 |
| hgdp | rs7797466 |
| ensembl | rs7797466 |
| geneview | rs7797466 |
| scholar | rs7797466 |
| rs7797466 | |
| pharmgkb | rs7797466 |
| gwascentral | rs7797466 |
| openSNP | rs7797466 |
| 23andMe | rs7797466 |
| SNPshot | rs7797466 |
| SNPdbe | rs7797466 |
| MSV3d | rs7797466 |
| GWAS Ctlg | rs7797466 |
| GMAF | 0.208 |
| Max Magnitude | 0 |
| ? | (A;A) (A;G) (G;G) | 28 |
|---|---|---|
|
| ||
The observed association of rs7797466 with ovarian cancer warrants confirmation in an independent study [PMID 16774946].
- rs7797466 PMS2 rs7797466 may have a role in development of ovarian cancer
[PMID 19543528
] Association between common germline genetic variation in 94 candidate genes or regions and risks of invasive epithelial ovarian cancer.
