ClinVar Miner

List of variants reported as benign for RPGR-related retinopathy by Fulgent Genetics, Fulgent Genetics

Included ClinVar conditions (7):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
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_001034853.2(RPGR):c.223A>G (p.Ile75Val)	rs111631988	0.03363
NM_001034853.2(RPGR):c.552G>T (p.Gln184His)	rs5963403	0.02128

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