rs397507890(TTTCGG;TTTCGG)
From SNPedia
common in clinvar |
Is a | genotype |
of | rs397507890 |
Gene | BRCA2 |
Chromosome | 13 |
Position | 32,346,893 |
mentioned | by |
Magnitude | 0 |
Repute | Good |
Geno | Mag | Summary |
---|---|---|
(-;TTCGGT) | 6 | BRCA2 variant considered pathogenic for breast cancer |
(TTCGGT;TTCGGT) | 0 | common in clinvar |
(TTTCGG;TTTCGG) | 0 | common in clinvar |