List of variants reported as uncertain significance for intestinal neoplasm by Foundation for Research in Genetics and Endocrinology, FRIGE's Institute of Human Genetics

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_000179.3(MSH6):c.3788G>A (p.Arg1263His)	rs147852216	0.00010
NM_000251.3(MSH2):c.274C>G (p.Leu92Val)	rs587779154	0.00001
NM_000179.3(MSH6):c.2365A>C (p.Asn789His)	rs2104402954
NM_000249.4(MLH1):c.200G>T (p.Gly67Val)	rs63749939
NM_000249.4(MLH1):c.884+6G>A	rs1575496158
NM_000251.3(MSH2):c.2551C>G (p.Leu851Val)	rs267608015
NM_001040108.2(MLH3):c.2312A>T (p.Glu771Val)
NM_002354.3(EPCAM):c.214G>A (p.Glu72Lys)

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