"Human Genome and Stem Cell Research Center, Department of Genetics an - ClinVar

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	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 2497703	NM_014838.3(ZBED4):c.1006C>G (p.Arg336Gly)	ALG12, ZBED4 (R336G)	Single nucleotide variant (missense variant)	not provided	GUncertain significance
Select item 223119	Single allele	DENND6B, TYMP +34 more	Deletion	Autism spectrum disorder +1 more	GPathogenic
Select item 223118	Single allele	PANX2, PIM3 +33 more	Deletion	Autism spectrum disorder	GPathogenic

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