List of variants in gene ATP6AP2 reported as likely benign for basal ganglia 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: 2

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HGVS	dbSNP	gnomAD frequency
NM_005765.3(ATP6AP2):c.38-5T>C	rs190477001	0.00243
NM_005765.3(ATP6AP2):c.1050T>C (p.Asp350=)	rs79790275	0.00141

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