C3806722[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 136465	NM_005765.3(ATP6AP2):c.38-5T>C	ATP6AP2	Single nucleotide variant (intron variant)	Syndromic X-linked intellectual disability Hedera type +4 more	GBenign/Likely benign
Select item 199113	NM_005765.3(ATP6AP2):c.1050T>C (p.Asp350=)	ATP6AP2	Single nucleotide variant (synonymous variant)	not specified +3 more	GBenign/Likely benign