List of variants reported as pathogenic for autosomal recessive nonsyndromic hearing loss 63

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Total variants: 8

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HGVS	dbSNP	gnomAD frequency
NM_001393500.2(TOMT):c.229G>A (p.Glu77Lys)	rs137853187	0.00004
NM_001393500.2(TOMT):c.259+4A>C	rs545947177	0.00002
NM_001393500.2(TOMT):c.143G>A (p.Arg48Gln)	rs137853185	0.00001
NM_001393500.2(TOMT):c.100C>T (p.Arg34Ter)
NM_001393500.2(TOMT):c.214T>C (p.Trp72Arg)	rs137853186
NM_001393500.2(TOMT):c.234C>G (p.Tyr78Ter)	rs137853188
NM_001393500.2(TOMT):c.515_518dup (p.Ser174fs)	rs797044907
NM_145309.6(LRRC51):c.340_346del (p.Ile114fs)	rs759544282

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