List of variants reported as likely pathogenic for colorectal cancer by Centre for Mendelian Genomics, University Medical Centre Ljubljana

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000535.7(PMS2):c.2249G>A (p.Gly750Asp)	rs587779337	0.00001
NM_000535.7(PMS2):c.825A>G (p.Gln275=)	rs876659736	0.00001
NM_000179.3(MSH6):c.2906A>G (p.Tyr969Cys)	rs63749919
NM_000249.4(MLH1):c.1896G>C (p.Glu632Asp)
NM_000535.7(PMS2):c.2007-2A>G	rs587782336

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