List of variants in gene combination ACTC1, GJD2-DT reported as uncertain significance by Clinical Molecular Genetics Laboratory, Johns Hopkins All Children's Hospital

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_005159.5(ACTC1):c.56_57insCA (p.Lys20fs)	rs730880387	0.00004
NM_005159.5(ACTC1):c.101C>T (p.Pro34Leu)	rs1373760624
NM_005159.5(ACTC1):c.922T>A (p.Tyr308Asn)	rs1566967093

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