rs397507753(TCAG;TCAG)
From SNPedia
| common in clinvar |
| Is a | genotype |
| of | rs397507753 |
| Gene | BRCA2 |
| Chromosome | 13 |
| Position | 32,339,342 |
| mentioned | by |
| Magnitude | 0 |
| Repute | Good |
| Geno | Mag | Summary |
|---|---|---|
| (-;GTCA) | 6 | BRCA2 variant considered pathogenic for breast cancer |
| (GTCA;GTCA) | 0 | common in clinvar |
| (TCAG;TCAG) | 0 | common in clinvar |
