List of variants reported as pathogenic for colorectal cancer by Center for Human Genetics, Inc, Center for Human Genetics, Inc

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Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3743_3744insT (p.Tyr1249fs)	rs786201084
NM_000179.3(MSH6):c.3959_3962del (p.Ala1320fs)	rs267608120
NM_000249.4(MLH1):c.1381A>T (p.Lys461Ter)	rs63750540
NM_000249.4(MLH1):c.1500_1502del (p.Ile501del)	rs587778920
NM_000249.4(MLH1):c.589C>T (p.Gln197Ter)	rs1553644123
NM_000251.3(MSH2):c.289C>T (p.Gln97Ter)	rs63750970

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