C4747517[trait identifier] AND "Kids Research, The Children's Hospital - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 869392	NM_014049.5(ACAD9):c.632A>G (p.Lys211Arg)	ACAD9 (K211R)	Single nucleotide variant (missense variant +1 more)	Acyl-CoA dehydrogenase 9 deficiency	GLikely pathogenic
Select item 30882	NM_014049.5(ACAD9):c.797G>A (p.Arg266Gln)	ACAD9 (R266Q)	Single nucleotide variant (missense variant +1 more)	not provided +1 more	GPathogenic
Select item 869393	NM_014049.5(ACAD9):c.842C>T (p.Pro281Leu)	ACAD9 (P281L)	Single nucleotide variant (missense variant +1 more)	Acyl-CoA dehydrogenase 9 deficiency	GLikely pathogenic

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ClinVar