"Fulgent Genetics, Fulgent Genetics"[submitter] AND "RP2"[gene] - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 636099	NM_006915.3(RP2):c.49C>T (p.Pro17Ser)	LOC130068202, RP2 (P17S)	Single nucleotide variant (missense variant)	Retinitis pigmentosa 2 +1 more	GUncertain significance
Select item 1011905	NM_006915.3(RP2):c.286G>A (p.Val96Met)	RP2 (V96M)	Single nucleotide variant (missense variant)	Inborn genetic diseases +2 more	GUncertain significance
Select item 737352	NM_006915.3(RP2):c.751A>G (p.Arg251Gly)	RP2 (R251G)	Single nucleotide variant (missense variant)	Retinitis pigmentosa 2 +1 more	GBenign/Likely benign
Select item 764245	NM_006915.3(RP2):c.1001C>A (p.Ser334Tyr)	RP2 (S334Y)	Single nucleotide variant (missense variant)	Retinitis pigmentosa 2 +2 more	GBenign/Likely benign

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