List of variants in gene combination ACTC1, GJD2-DT reported as pathogenic for not provided

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_005159.5(ACTC1):c.301G>A (p.Glu101Lys)	rs193922680	0.00001
NM_005159.5(ACTC1):c.383C>T (p.Thr128Ile)	rs727504308
NM_005159.5(ACTC1):c.811A>G (p.Met271Val)	rs2140429730
NM_005159.5(ACTC1):c.968C>T (p.Ala323Val)	rs730880404

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