"NIHR Bioresource Rare Diseases, University of Cambridge"[submitter] A - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 437942	NM_006915.3(RP2):c.11TCT[1] (p.Phe5del)	LOC130068202, RP2 (F5del)	Microsatellite (inframe_deletion)	Cone-rod dystrophy +2 more	GConflicting classifications of pathogenicity
Select item 437945	NM_006915.3(RP2):c.43del (p.Ser15fs)	LOC130068202, RP2 (S15fs)	Deletion (frameshift variant)	Abnormality of the eye	GLikely pathogenic