List of variants in gene RPGRIP1 reported by Ophthalmic Genetics Group, Institute of Molecular and Clinical Ophthalmology Basel

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Gene type: Distinguish antisense genes from sense genes
		ClinVar version:

Total variants: 4

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HGVS	dbSNP	gnomAD frequency
NM_020366.4(RPGRIP1):c.2895+1G>T	rs748072501	0.00001
NM_020366.4(RPGRIP1):c.2941C>T (p.Arg981Ter)	rs780667159	0.00001
NM_020366.4(RPGRIP1):c.2367+23del	rs781728563
NM_020366.4(RPGRIP1):c.2480G>T (p.Arg827Leu)	rs28937883

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