ClinVar Miner

List of variants reported as uncertain significance for Familial adenomatous polyposis 2 by Center for Human Genetics, Inc, Center for Human Genetics, Inc

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Show significances as they were submitted (without aggregation into standard terms)
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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_001048174.2(MUTYH):c.583A>G (p.Ile195Val)	rs200872702	0.00009
NM_001048174.2(MUTYH):c.379-4A>G	rs1553129371

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