List of variants reported as likely pathogenic for colorectal cancer by Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_000249.4(MLH1):c.2038T>G (p.Cys680Gly)	rs63750809	0.00007
NC_000002.12:g.(47369582_47373462)_(47386613_?)del
NC_000002.12:g.(47369582_47373462)_(47386896_?)del
NC_000003.12:g.(?_37040183)_(37063791_?)del
NM_000249.4(MLH1):c.306G>T (p.Glu102Asp)	rs63751665

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