rs80359530(CT;CT)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs80359530 |
| Gene | BRCA2 |
| Chromosome | 13 |
| Position | 32,340,073 |
| Merged from | Rs80359531 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;CT) | 6 | Possible miscall in Ancestry data; otherwise, BRCA2 variant considered pathogenic for breast cancer |
| (-;CTCT) | 6 | Possible miscall in Ancestry data; otherwise, BRCA2 variant considered pathogenic for breast cancer |
| (CT;CT) | 0 | common in clinvar |
| (CTCT;CTCT) | 0 | common/normal |
