C0339573[trait identifier] AND "Fulgent Genetics, Fulgent Genetics"[su - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 7099	NM_001008212.2(OPTN):c.293T>A (p.Met98Lys)	LOC108903148, OPTN (M98K)	Single nucleotide variant (missense variant)	not specified +5 more	GBenign/Likely benign
Select item 299210	NM_001008212.2(OPTN):c.402C>A (p.Ala134=)	OPTN	Single nucleotide variant (synonymous variant)	Inborn genetic diseases +5 more	GBenign/Likely benign
Select item 126958	NM_000428.3(LTBP2):c.4912G>A (p.Val1638Met)	LTBP2 (V1638M)	Single nucleotide variant (missense variant)	Glaucoma 3, primary congenital, D +4 more	GUncertain significance

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