ClinVar Miner

List of variants in gene ROGDI reported as likely benign by Center for Pediatric Genomic Medicine, Children's Mercy Hospital and Clinics

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_024589.3(ROGDI):c.713G>A (p.Arg238His)	rs138409264	0.00548
NM_024589.3(ROGDI):c.117+10C>G	rs113858060

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