C4014435[trait identifier] AND "Institute of Human Genetics, Heidelber - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 1174542	NM_015570.4(AUTS2):c.1A>T (p.Met1Leu)	AUTS2 (M1L)	Single nucleotide variant (missense variant +1 more)	Autism spectrum disorder due to AUTS2 deficiency	GPathogenic
Select item 981243	Single allele	AUTS2	Deletion	Autism spectrum disorder due to AUTS2 deficiency	GPathogenic