C0004352[trait identifier] AND "Laboratorio de Genetica Humana; Univer - ClinVar - NCBI

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Items: 4

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 212706	NM_006186.4(NR4A2):c.357G>T (p.Ser119=)	NR4A2	Single nucleotide variant (synonymous variant)	Autism	GBenign
Select item 212709	NM_000693.4(ALDH1A3):c.1514T>C (p.Ile505Thr)	ALDH1A3, ALDH1A3-AS1 (I505T +1 more)	Single nucleotide variant (non-coding transcript variant +1 more)	Autism	GLikely pathogenic
Select item 212708	NM_001481.3(GAS8):c.90+1487_90+1488insGCTGCCCCGCAG	GAS8, GAS8-AS1	Insertion (non-coding transcript variant +1 more)	Autism	GLikely benign
Select item 212710	NM_001369369.1(FOXN1):c.146C>T (p.Ser49Leu)	FOXN1 (S49L)	Single nucleotide variant (missense variant)	Autism	GLikely pathogenic

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