C4310817[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 714911	NM_001368397.1(FRMPD4):c.741C>G (p.Leu247=)	FRMPD4	Single nucleotide variant (synonymous variant)	not provided +1 more	GBenign/Likely benign
Select item 739255	NM_001368397.1(FRMPD4):c.1224T>C (p.His408=)	FRMPD4	Single nucleotide variant (synonymous variant)	not provided +2 more	GBenign/Likely benign
Select item 254683	NM_001368397.1(FRMPD4):c.1657T>C (p.Cys553Arg)	FRMPD4 (C553R +5 more)	Single nucleotide variant (missense variant)	Intellectual disability, X-linked 104	GLikely pathogenic

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