ClinVar Miner

List of variants reported as likely pathogenic for autism spectrum disorder due to AUTS2 deficiency by Dobyns Lab, Seattle Children's Research Institute

Included ClinVar conditions (2):

Minimum submission review status:		Collection method:
Minimum conflict level: Report conflict between different conditions
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants: 1

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HGVS	dbSNP	gnomAD frequency
NM_015570.4(AUTS2):c.1600A>C (p.Thr534Pro)	rs1563183469

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