List of variants reported as pathogenic for Autosomal dominant nonsyndromic hearing loss 20; Baraitser-winter syndrome 2 by Labcorp Genetics (formerly Invitae), Labcorp

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001614.5(ACTG1):c.151G>A (p.Asp51Asn)
NM_001614.5(ACTG1):c.548G>A (p.Arg183Gln)	rs781945750
NM_001614.5(ACTG1):c.721G>A (p.Glu241Lys)	rs267606631
NM_001614.5(ACTG1):c.760C>T (p.Arg254Trp)	rs281875328
NM_001614.5(ACTG1):c.833C>T (p.Thr278Ile)	rs28999112
NM_001614.5(ACTG1):c.914T>C (p.Met305Thr)
NM_001614.5(ACTG1):c.94C>T (p.Pro32Ser)	rs1598551290
NM_001614.5(ACTG1):c.994C>G (p.Pro332Ala)	rs104894545

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