List of variants in gene RDX reported as likely pathogenic for autosomal recessive nonsyndromic hearing loss 24

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Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 6

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HGVS	dbSNP	gnomAD frequency
NM_002906.4(RDX):c.1135C>T (p.Arg379Ter)	rs772146113	0.00001
NM_002906.4(RDX):c.-64-1215_12+348del
NM_002906.4(RDX):c.1076_1079del (p.Ile359fs)
NM_002906.4(RDX):c.1141C>T (p.Arg381Ter)	rs1308348441
NM_002906.4(RDX):c.295C>T (p.Gln99Ter)
NM_002906.4(RDX):c.513_514del (p.Arg171fs)	rs2134364635

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