List of variants in gene RDX reported as pathogenic by Labcorp Genetics (formerly Invitae), Labcorp

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: 3

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HGVS	dbSNP	gnomAD frequency
NM_002906.4(RDX):c.484_487del (p.His161_Lys162insTer)	rs2539423213
NM_002906.4(RDX):c.682_685del (p.Tyr228fs)	rs2134363728
NM_002906.4(RDX):c.930_931del (p.Glu311fs)	rs2539410522

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