RS63749831 MSH2
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What This Variant Does
"rs63749831, also known as c.1786_1788delAAT, p.Asn596del and N596del, is a very rare mutation in the...
Associated Conditions
Lynch syndrome 1
Lynch syndrome
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Carcinoma of colon
MSH2-related disorder
Lynch syndrome 1
Lynch syndrome
Hereditary cancer-predisposing syndrome
Hereditary nonpolyposis colorectal neoplasms
Carcinoma of colon
MSH2-related disorder
Other Variants in MSH2