C3150691[trait identifier] AND "3billion"[submitter] - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2444372	NM_001029883.3(PCARE):c.3048_3049del (p.Tyr1016_Arg1017delinsTer)	PCARE	Deletion (nonsense)	Retinitis pigmentosa 54	GLikely pathogenic
Select item 841159	NM_001029883.3(PCARE):c.1837C>T (p.Arg613Ter)	PCARE (R613*)	Single nucleotide variant (nonsense)	Retinitis pigmentosa 54 +1 more	GPathogenic
Select item 866068	NM_001029883.3(PCARE):c.958del (p.Arg320fs)	PCARE (R320fs)	Deletion (frameshift variant)	not provided +3 more	GPathogenic/Likely pathogenic

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