rs397509136(A;G)
From SNPedia
| BRCA1 variant of unclear significance |
| Is a | genotype |
| of | rs397509136 |
| Gene | BRCA1 |
| Chromosome | 17 |
| Position | 43,091,459 |
| mentioned | by |
| Magnitude | 3 |
| Repute | Bad |
| Geno | Mag | Summary |
|---|---|---|
| (A;G) | 3 | BRCA1 variant of unclear significance |
| (G;G) | 0 | common in clinvar |
| (G;T) | 6 | BRCA1 variant considered pathogenic for breast cancer |
see discussion at rs397509136
