List of variants in gene MUTYH reported as pathogenic for Familial colorectal cancer

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.1103G>A (p.Gly368Asp)	rs36053993	0.00341
NM_001048174.2(MUTYH):c.649C>T (p.Arg217Cys)	rs200495564	0.00002
NM_001048174.2(MUTYH):c.1087C>T (p.Gln363Ter)	rs587783057	0.00001
NM_001048174.2(MUTYH):c.228C>A (p.Tyr76Ter)	rs121908380

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