RS150766139 NTHL1;TSC2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Familial adenomatous polyposis 3
Hereditary cancer-predisposing syndrome
NTHL1-related disorder
Inherited polyposis and early onset colorectal cancer - germline testing
Colorectal cancer
Familial adenomatous polyposis 3
Hereditary cancer-predisposing syndrome
NTHL1-related disorder
Inherited polyposis and early onset colorectal cancer - germline testing
Colorectal cancer
Other Variants in NTHL1;TSC2