List of variants in gene RGR reported as likely pathogenic for inborn disorder of amino acid metabolism

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_001012720.2(RGR):c.236G>A (p.Arg79Gln)	rs761554381	0.00003
NM_001012720.2(RGR):c.196A>C (p.Ser66Arg)	rs104894187	0.00002
NM_001012720.2(RGR):c.820del (p.Arg274fs)	rs1589337745

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