RS141568342 CHEK2
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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
Breast and colorectal cancer
susceptibility to
Familial cancer of breast
Malignant tumor of breast
Breast and/or ovarian cancer
Hereditary breast ovarian cancer syndrome
Predisposition to cancer
CHEK2-related cancer predisposition
CHEK2-related disorder
Bone osteosarcoma
Familial prostate cancer
Neoplasm
Hereditary cancer-predisposing syndrome
Breast and colorectal cancer
Other Variants in CHEK2