RS587782537 MSH2

Health Risk Chr 2:47412443
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What This Variant Does
"CLNSIG=5
Associated Conditions
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome 1
Muir-Torré syndrome
Mismatch repair cancer syndrome 2
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome 1
Muir-Torré syndrome
Mismatch repair cancer syndrome 2
Other Variants in MSH2
rs28929483 rs63751108 rs28929484 rs63749831 rs63750047 rs63751207 rs63749811 rs1553350126 rs63750875 rs63751449
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