C4225256[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 464827	NM_033453.4(ITPA):c.124C>T (p.Leu42=)	ITPA	Single nucleotide variant (5 prime UTR variant +3 more)	Inosine triphosphatase deficiency +2 more	GLikely benign
Select item 445902	NM_033453.4(ITPA):c.278A>G (p.Glu93Gly)	ITPA (E93G +2 more)	Single nucleotide variant (missense variant +2 more)	Inosine triphosphatase deficiency +3 more	GBenign/Likely benign