List of variants reported as likely pathogenic for nonsyndromic genetic hearing loss by Institute of Medical Genetics and Applied Genomics, University Hospital Tübingen

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Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001256317.3(TMPRSS3):c.1340T>C (p.Met447Thr)	rs201018751	0.00001
NM_000441.2(SLC26A4):c.584T>C (p.Leu195Pro)
NM_005982.4(SIX1):c.316G>T (p.Val106Leu)	rs2140241235

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