List of variants in gene RPGRIP1 reported as pathogenic by Rui Chen Lab, Baylor College of Medicine

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_020366.4(RPGRIP1):c.564A>G (p.Glu188=)	rs574462207	0.00001
NM_020366.4(RPGRIP1):c.1611G>A (p.Gln537=)	rs1064797181
NM_020366.4(RPGRIP1):c.3339+5G>A	rs1057518122

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