ClinVar Miner

List of variants reported as pathogenic for RPGR-related retinopathy by Institute of Human Genetics, University Hospital Muenster

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.2257_2260del (p.Gly753fs)	rs2067187618
NM_001034853.2(RPGR):c.2916_2917del (p.Glu973fs)	rs2067140574

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