C2681923[trait identifier] AND "Ocular Genomics Institute, Massachuset - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1065686	NM_006915.3(RP2):c.103-2A>G	RP2	Single nucleotide variant (splice acceptor variant)	Retinitis pigmentosa 2	GLikely pathogenic
Select item 866167	NM_006915.3(RP2):c.768G>C (p.Glu256Asp)	RP2 (E256D)	Single nucleotide variant (missense variant)	not provided +2 more	GConflicting classifications of pathogenicity
Select item 1043015	NM_006915.3(RP2):c.969+2T>C	RP2	Single nucleotide variant (splice donor variant)	not provided +1 more	GPathogenic/Likely pathogenic

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