List of variants in gene RDX reported as likely benign for Nonsyndromic Hearing Loss, Recessive

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_002906.4(RDX):c.*1260GT[12]	rs61030269
NM_002906.4(RDX):c.523_524del	rs144848373
NM_002906.4(RDX):c.*923del	rs35381725
NM_002906.4(RDX):c.-64-6del	rs61003001

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