RS587781410 RAD51C
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What This Variant Does
"Mentioned as a pathogenic/likely pathogenic mutation associated with cancer predisposition in
Associated Conditions
Hereditary cancer-predisposing syndrome
Fanconi anemia complementation group O
Breast-ovarian cancer
familial
susceptibility to
3
Hereditary site-specific ovarian cancer syndrome
Hereditary breast ovarian cancer syndrome
Breast and/or ovarian cancer
Uterine corpus cancer
Hereditary cancer
Inherited breast cancer and ovarian cancer
RAD51C-related cancer predisposition
Hereditary cancer-predisposing syndrome
Fanconi anemia complementation group O
Other Variants in RAD51C