RS63750778 MSH2
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What This Variant Does
"CLNSIG=5
Associated Conditions
Lynch syndrome
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome 1
MSH2-related disorder
Mismatch repair cancer syndrome 2
Muir-Torré syndrome
Inherited MMR deficiency (Lynch syndrome)
Hereditary nonpolyposis colorectal neoplasms
Hereditary cancer-predisposing syndrome
Lynch syndrome
Lynch syndrome
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome 1
Other Variants in MSH2