C1851481[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 137205	NM_022726.4(ELOVL4):c.814G>C (p.Glu272Gln)	ELOVL4 (E272Q)	Single nucleotide variant (missense variant)	not provided +4 more	GBenign/Likely benign
Select item 143056	NM_022726.4(ELOVL4):c.504G>C (p.Leu168Phe)	ELOVL4 (L168F)	Single nucleotide variant (missense variant)	Stargardt disease 3 +3 more	GPathogenic
Select item 358148	NM_022726.4(ELOVL4):c.351T>A (p.Asn117Lys)	ELOVL4 (N117K)	Single nucleotide variant (missense variant)	Stargardt disease 3 +4 more	GConflicting classifications of pathogenicity

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ClinVar