RS267607939 MSH2
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What This Variant Does
"CLNSIG=4
Associated Conditions
Hereditary cancer-predisposing syndrome
Papillary renal cell carcinoma type 1
Lynch syndrome 1
Mismatch repair cancer syndrome 1
Muir-Torré syndrome
Hereditary nonpolyposis colorectal neoplasms
Hereditary nonpolyposis colon cancer
Hereditary breast ovarian cancer syndrome
Lynch syndrome
Endometrial carcinoma
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome 1
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome 1
Other Variants in MSH2