RS587779243 MSH6
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What This Variant Does
"rs587779243, also known as c.2569_2572delGATT or p.Asp857Phefs, represents a pathogenic mutation for...
Associated Conditions
Lynch syndrome
Carcinoma of colon
Ovarian carcinoma
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome 5
Mismatch repair cancer syndrome 3
Lynch syndrome
Carcinoma of colon
Ovarian carcinoma
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Lynch syndrome 5
Mismatch repair cancer syndrome 3
Other Variants in MSH6