List of variants reported as pathogenic for autosomal recessive nonsyndromic hearing loss 15

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Total variants: 7

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HGVS	dbSNP	gnomAD frequency
NM_133261.3(GIPC3):c.136G>A (p.Gly46Arg)	rs946085339	0.00002
NM_133261.3(GIPC3):c.565C>T (p.Arg189Cys)	rs387907002
NM_133261.3(GIPC3):c.685dup (p.Ala229fs)	rs748150647
NM_133261.3(GIPC3):c.724G>T (p.Glu242Ter)	rs1568278651
NM_133261.3(GIPC3):c.767G>A (p.Gly256Asp)	rs387907001
NM_133261.3(GIPC3):c.785T>G (p.Leu262Arg)	rs387906999
NM_133261.3(GIPC3):c.903G>A (p.Trp301Ter)	rs387907000

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