RS730882048 XRCC2

Health Risk Chr 7:152660726
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
Breast carcinoma
Malignant tumor of unknown origin
Hereditary cancer-predisposing syndrome
Breast carcinoma
Malignant tumor of unknown origin
Other Variants in XRCC2
rs143153871 rs140214637 rs587780129 rs61762969 rs368445278 rs149186933 rs56103026 rs149099078 rs730882046 rs730882040
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