RS63749900 MLH1
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome
Mismatch repair cancer syndrome 1
Colorectal cancer
hereditary nonpolyposis
type 2
Muir-Torré syndrome
Lynch syndrome
Hereditary nonpolyposis colorectal neoplasms
Hereditary cancer-predisposing syndrome
Colorectal cancer
hereditary nonpolyposis
type 2
Inherited MMR deficiency (Lynch syndrome)
Other Variants in MLH1