List of variants reported as uncertain significance for colorectal cancer by Division of Medical Genetics, University of Washington

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Total variants: 15

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HGVS	dbSNP	gnomAD frequency
NM_000251.3(MSH2):c.818T>C (p.Val273Ala)	rs144288433	0.00007
NM_000251.3(MSH2):c.1121A>G (p.Gln374Arg)	rs749660228	0.00004
NM_000251.3(MSH2):c.1189C>G (p.Gln397Glu)	rs63750611	0.00004
NM_000179.3(MSH6):c.1120_1122del (p.Lys374del)	rs587781660	0.00003
NM_000249.4(MLH1):c.991G>A (p.Glu331Lys)	rs550914672	0.00003
NM_000251.3(MSH2):c.1681G>A (p.Glu561Lys)	rs63750328	0.00002
NM_000179.3(MSH6):c.2282G>C (p.Arg761Thr)	rs587779233	0.00001
NM_000249.4(MLH1):c.1460G>A (p.Arg487Gln)	rs587778917	0.00001
NM_000251.3(MSH2):c.2048G>T (p.Gly683Val)	rs755920849	0.00001
NM_000251.3(MSH2):c.362A>G (p.Tyr121Cys)	rs587779971	0.00001
NM_000535.7(PMS2):c.1262G>A (p.Arg421Gln)	rs778482303	0.00001
NM_000179.3(MSH6):c.2426T>C (p.Val809Ala)	rs775815297
NM_000251.3(MSH2):c.2567A>G (p.Tyr856Cys)	rs587779150
NM_000535.7(PMS2):c.2143C>T (p.His715Tyr)	rs747494931
NM_000535.7(PMS2):c.551T>C (p.Met184Thr)	rs1583387794

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