List of variants reported as pathogenic for hearing loss, autosomal dominant 76 by OMIM

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Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_001145319.2(PLS1):c.1087C>T (p.Leu363Phe)	rs1560070780
NM_001145319.2(PLS1):c.383T>C (p.Phe128Ser)	rs1577876794
NM_001145319.2(PLS1):c.713T>G (p.Leu238Arg)	rs1577888561
NM_001145319.2(PLS1):c.805G>A (p.Glu269Lys)	rs1577888985

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