List of variants reported as uncertain significance for autosomal dominant nonsyndromic hearing loss by Bioscientia Institut fuer Medizinische Diagnostik GmbH, Sonic Healthcare

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Total variants: 2

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HGVS	dbSNP	gnomAD frequency
NM_005219.5(DIAPH1):c.2082G>T (p.Leu694Phe)	rs778995744	0.00001
NM_005422.4(TECTA):c.458C>T (p.Thr153Met)	rs1555121799

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