rs397509007(-;CT)
From SNPedia
BRCA1 variant considered pathogenic for breast cancer |
Is a | genotype |
of | rs397509007 |
Gene | BRCA1 |
Chromosome | 17 |
Position | 43,092,786 |
Merged into | Rs80357540 |
mentioned | by |
Magnitude | 6 |
Repute | Bad |
Geno | Mag | Summary |
---|---|---|
(-;CT) | 6 | BRCA1 variant considered pathogenic for breast cancer |
(CT;CT) | 0 | common in clinvar |
see details via ClinVar sidebar/box on associated SNP/rs# page