List of variants reported as uncertain significance for Autosomal recessive nonsyndromic hearing loss 18A by Baylor Genetics

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_153676.4(USH1C):c.2611G>A (p.Ala871Thr)	rs56165709	0.00336
NM_153676.4(USH1C):c.1910C>G (p.Thr637Ser)	rs754365594
NM_153676.4(USH1C):c.2520C>A (p.Cys840Ter)
NM_153676.4(USH1C):c.2535T>A (p.Tyr845Ter)
NM_153676.4(USH1C):c.2546+1G>A

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