List of variants in gene RPGRIP1 reported as pathogenic by Institute of Vision Research, Yonsei University 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_020366.3(RPGRIP1):c.[2302C>T];[3565_3571del]
NM_020366.4(RPGRIP1):c.3565_3571del (p.Arg1189fs)	rs587783012
NM_020366.4(RPGRIP1):c.[2079C>G];[2212_2215+21del]

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