RS774281788 ATM
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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
Ataxia-telangiectasia syndrome
Hereditary cancer
Familial cancer of breast
Malignant tumor of breast
Hereditary breast ovarian cancer syndrome
Familial colorectal cancer type X
Hereditary cancer-predisposing syndrome
Ataxia-telangiectasia syndrome
Hereditary cancer
Familial cancer of breast
Malignant tumor of breast
Hereditary breast ovarian cancer syndrome
Familial colorectal cancer type X
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