List of variants reported as pathogenic for colorectal cancer by Diagnostic Laboratory, Department of Genetics, University Medical Center Groningen

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Total variants: 9

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3202C>T (p.Arg1068Ter)	rs63749843	0.00002
NM_000535.7(PMS2):c.1882C>T (p.Arg628Ter)	rs63750451	0.00002
NM_000179.3(MSH6):c.2731C>T (p.Arg911Ter)	rs63751017	0.00001
NM_000179.3(MSH6):c.651dup (p.Lys218Ter)	rs63750955	0.00001
NM_000179.3(MSH6):c.3838C>T (p.Gln1280Ter)	rs63750139
NM_000249.4(MLH1):c.1896G>A (p.Glu632=)	rs63751632
NM_000249.4(MLH1):c.545+3A>G	rs267607760
NM_000251.3(MSH2):c.1861C>T (p.Arg621Ter)	rs63750508
NM_000251.3(MSH2):c.2633_2634del (p.Glu878fs)	rs63751618

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