C0004352[trait identifier] AND "Lyon Laboratory, Cold Spring Harbor La - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 203994	NM_000228.3(LAMB3):c.133T>G (p.Ser45Ala)	LAMB3 (S45A)	Single nucleotide variant (missense variant)	Autism	GUncertain significance
Select item 204362	Single allele	ALG1L2	Deletion	Autism	GUncertain significance
Select item 204363	Single allele	LOC129992127	Deletion	Autism	GUncertain significance
Select item 204361	Single allele		Deletion	Autism	GUncertain significance
Select item 203993	NM_014520.4(MYBBP1A):c.139C>T (p.Gln47Ter)	MYBBP1A (Q47*)	Single nucleotide variant (nonsense)	Autism	GUncertain significance

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