C3715216[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1463164	NM_002900.3(RBP3):c.722A>T (p.Asp241Val)	RBP3 (D241V)	Single nucleotide variant (missense variant)	Retinitis pigmentosa 66 +2 more	GUncertain significance
Select item 779143	NM_002900.3(RBP3):c.1296G>A (p.Val432=)	RBP3	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa +2 more	GBenign/Likely benign
Select item 725981	NM_002900.3(RBP3):c.1503C>T (p.Ala501=)	RBP3	Single nucleotide variant (synonymous variant)	Retinitis pigmentosa 66 +2 more	GBenign/Likely benign
Select item 193238	NM_002900.3(RBP3):c.2650G>A (p.Val884Met)	RBP3 (V884M)	Single nucleotide variant (missense variant)	Retinal dystrophy +4 more	GBenign/Likely benign

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