rs397507830(A;A)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs397507830 |
Gene | BRCA2 |
Chromosome | 13 |
Position | 32,326,595 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(-;-) | 0 | common in clinvar |
(-;CTTA) | 6 | BRCA2 variant considered pathogenic for breast cancer |
(-;TGAG) | 6 | BRCA2 variant considered pathogenic for breast cancer |
(A;A) | 0 | common in clinvar |