List of variants in gene RDX reported as uncertain significance by GeneDx

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: 26

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HGVS	dbSNP	gnomAD frequency
NM_002906.4(RDX):c.1106C>G (p.Thr369Ser)	rs201399984	0.00033
NM_002906.4(RDX):c.1037A>C (p.Glu346Ala)	rs141462728	0.00018
NM_002906.4(RDX):c.1154A>C (p.Glu385Ala)	rs146713867	0.00015
NM_002906.4(RDX):c.256C>G (p.Pro86Ala)	rs376418131	0.00011
NM_002906.4(RDX):c.1688A>G (p.Lys563Arg)	rs139896690	0.00009
NM_002906.4(RDX):c.778A>G (p.Ile260Val)	rs138116275	0.00007
NM_002906.4(RDX):c.146A>G (p.Tyr49Cys)	rs201338088	0.00006
NM_002906.4(RDX):c.1024C>T (p.Arg342Cys)	rs1030064754	0.00002
NM_002906.4(RDX):c.413A>G (p.Asn138Ser)	rs190296143	0.00002
NM_002906.4(RDX):c.1364A>C (p.Asp455Ala)	rs727505062	0.00001
NM_002906.4(RDX):c.1522C>T (p.His508Tyr)	rs751403876	0.00001
NM_002906.4(RDX):c.401A>G (p.Tyr134Cys)	rs768988858	0.00001
NM_002906.4(RDX):c.766G>C (p.Val256Leu)	rs771731527	0.00001
NM_002906.4(RDX):c.1344+4A>G
NM_002906.4(RDX):c.1348T>C (p.Phe450Leu)
NM_002906.4(RDX):c.1384G>C (p.Glu462Gln)	rs2539358955
NM_002906.4(RDX):c.1411C>A (p.Pro471Thr)
NM_002906.4(RDX):c.1516A>G (p.Met506Val)
NM_002906.4(RDX):c.1567C>T (p.Arg523Cys)
NM_002906.4(RDX):c.1568G>A (p.Arg523His)	rs374217847
NM_002906.4(RDX):c.236A>G (p.Lys79Arg)	rs1346670512
NM_002906.4(RDX):c.263A>G (p.Asp88Gly)
NM_002906.4(RDX):c.394G>A (p.Ala132Thr)	rs2539440753
NM_002906.4(RDX):c.564G>C (p.Met188Ile)	rs141888853
NM_002906.4(RDX):c.773A>T (p.Lys258Met)
NM_002906.4(RDX):c.912G>A (p.Gln304=)

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