List of variants reported as pathogenic for autosomal recessive nonsyndromic hearing loss 16 by Genome-Nilou Lab

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Total variants: 5

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HGVS	dbSNP	gnomAD frequency
NM_153700.2(STRC):c.4057C>T (p.Gln1353Ter)	rs774312182	0.00011
NM_153700.2(STRC):c.4402C>T (p.Arg1468Ter)	rs377480477	0.00011
NM_153700.2(STRC):c.3670C>T (p.Arg1224Ter)	rs727503444	0.00007
NM_153700.2(STRC):c.4837G>T (p.Glu1613Ter)	rs769443188	0.00001
NM_153700.2(STRC):c.4251del (p.Leu1417_Leu1418insTer)	rs1366021609

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