List of variants in gene RPGRIP1 reported by NIHR Bioresource Rare Diseases, University of Cambridge

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: 6

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HGVS	dbSNP	gnomAD frequency
NM_020366.4(RPGRIP1):c.2398G>A (p.Glu800Lys)	rs565837539	0.00002
NM_020366.4(RPGRIP1):c.1116del (p.Lys372fs)	rs776880045
NM_020366.4(RPGRIP1):c.1152-1749_1763-1241del
NM_020366.4(RPGRIP1):c.2890del (p.Ser964fs)	rs1555302710
NM_020366.4(RPGRIP1):c.2941C>T (p.Arg981Ter)	rs780667159
NM_020366.4(RPGRIP1):c.3120G>A (p.Trp1040Ter)	rs1555303320

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