C1864723[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 223153	NM_018129.4(PNPO):c.674G>A (p.Arg225His)	PNPO (R225H)	Single nucleotide variant (missense variant)	Pyridoxal phosphate-responsive seizures +2 more	GPathogenic
Select item 589871	NM_018129.4(PNPO):c.697C>T (p.Arg233Trp)	PNPO (R233W)	Single nucleotide variant (missense variant)	Pyridoxal phosphate-responsive seizures +2 more	GUncertain significance