C4748135[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 1598717	NM_001190274.2(FBXO11):c.1617-4A>G	FBXO11	Single nucleotide variant (intron variant)	not provided +2 more	GBenign/Likely benign
Select item 1639995	NM_001190274.2(FBXO11):c.233-19T>C	FBXO11	Single nucleotide variant (intron variant)	Intellectual developmental disorder with dysmorphic facies and behavioral abnormalities +1 more	GLikely benign