C0004352[trait identifier] AND "Michaelson Lab, University of Iowa"[su - ClinVar - NCBI

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Items: 5

	Variation	Gene (Protein Change)	Type (Consequence)	Condition	Classification, Review status
Select item 590905	NM_001813.3(CENPE):c.3788C>G (p.Ala1263Gly)	CENPE (A1263G +1 more)	Single nucleotide variant (missense variant)	Autism	GUncertain significance
Select item 590906	NM_001204403.1(ANK3):c.-739C>T	ANK3, ANK3-DT	Single nucleotide variant	Autism	GUncertain significance
Select item 590907	NM_001330195.2(NRXN3):c.758-160258G>A	NRXN3	Single nucleotide variant (intron variant)	not provided	GBenign
Select item 590908	NM_001330195.2(NRXN3):c.3262+210045A>G	NRXN3	Single nucleotide variant (intron variant)	Autism	GUncertain significance
Select item 590909	Single allele		Deletion	Autism	GUncertain significance

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