List of variants in gene RGR reported as uncertain significance by Neuberg Centre For Genomic Medicine, NCGM

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.751G>A (p.Ala251Thr)	rs777299739	0.00003
NM_001012720.2(RGR):c.328G>A (p.Ala110Thr)	rs780231448	0.00001
NM_001012720.2(RGR):c.600G>T (p.Glu200Asp)

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