RS63750899 MLH1

Health Risk Chr 3:37048562
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What This Variant Does
"rs63750899 is a SNP in the MLH1 gene on chromosome 3, associated with Lynch syndrome (HNPCC). This v...
Associated Conditions
Colorectal cancer
hereditary nonpolyposis
type 2
Lynch syndrome
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Mismatch repair cancer syndrome 1
Hereditary nonpolyposis colorectal neoplasms
Hereditary cancer-predisposing syndrome
Hereditary cancer-predisposing syndrome
Colorectal cancer
hereditary nonpolyposis
type 2
Lynch syndrome
Hereditary cancer-predisposing syndrome
Other Variants in MLH1
rs63750198 rs63751109 rs63751247 rs863223312 rs63750710 rs63751615 rs63750206 rs63750781 rs63750691 rs63750217
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