RS63750047 MSH2
Upload your DNA to see your genotype for this variant.
What This Variant Does
"rs63750047 is a SNP in the MSH2 gene on chromosome 2, associated with Lynch syndrome (HNPCC). This v...
Associated Conditions
Muir-Torré syndrome
Lynch syndrome
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome 1
Muir-Torré syndrome
Lynch syndrome
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome 1
Other Variants in MSH2