RS587778134 BRIP1
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What This Variant Does
"rs587778134, also known as c.2040_2041insTT, c.2038_2039dupTT and p.Leu680Phefs, represents a rare m...
Associated Conditions
Hereditary cancer-predisposing syndrome
Fanconi anemia complementation group J
Familial cancer of breast
Breast and/or ovarian cancer
Uterine corpus cancer
Ovarian cancer
Fanconi anemia complementation group J
Familial cancer of breast
Hereditary cancer-predisposing syndrome
Fanconi anemia complementation group J
Familial cancer of breast
Breast and/or ovarian cancer
Uterine corpus cancer
Ovarian cancer
Fanconi anemia complementation group J
Other Variants in BRIP1