RS193922372 MSH2

Health Risk Chr 2:47429673
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What This Variant Does
"rs193922372, also known as c.1077-69_1143del136, represents a rare deletion variant in the MSH2 gene...
Associated Conditions
Lynch syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome
Hereditary nonpolyposis colorectal neoplasms
Other Variants in MSH2
rs28929483 rs63751108 rs28929484 rs63749831 rs63750047 rs63751207 rs63749811 rs1553350126 rs63750875 rs63751449
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