RS63751449 MSH2
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What This Variant Does
"rs63751449 is a SNP in the MSH2 gene on chromosome 2, associated with Lynch syndrome (HNPCC). This v...
Associated Conditions
Mismatch repair cancer syndrome 2
Lynch syndrome
Hereditary cancer-predisposing syndrome
Lynch syndrome 1
Mismatch repair cancer syndrome 2
Lynch syndrome
Hereditary cancer-predisposing syndrome
Lynch syndrome 1
Other Variants in MSH2