rs397507789(AAAAG;AAAAG)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs397507789 |
Gene | BRCA2 |
Chromosome | 13 |
Position | 32,339,935 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(-;AAAAG) | 6 | Miscall in 23andMe v4 data; otherwise, BRCA2 variant considered pathogenic for breast cancer |
(AAAAG;AAAAG) | 0 | common in clinvar |