List of variants in gene CTNNA1 reported as uncertain significance for Polyposis syndrome, hereditary mixed, 1

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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_001903.5(CTNNA1):c.339T>A (p.Asp113Glu)	rs773771416	0.00001
NM_001903.5(CTNNA1):c.1392del (p.Ile465fs)	rs2150233636
NM_001903.5(CTNNA1):c.1715T>C (p.Val572Ala)	rs2150289732
NM_001903.5(CTNNA1):c.2665A>G (p.Lys889Glu)	rs1766015674

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