List of variants in gene ATP6V0A1 reported as likely pathogenic for neurodevelopmental disorder

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

Total variants: 3

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HGVS	dbSNP	gnomAD frequency
NM_001130021.3(ATP6V0A1):c.118-1del
NM_001130021.3(ATP6V0A1):c.118-2A>G
NM_001130021.3(ATP6V0A1):c.2219G>A (p.Arg740Gln)	rs1567871600

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