List of variants in gene ATP6V1A reported as likely benign for eyelid 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: 1

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HGVS	dbSNP	gnomAD frequency
NM_001690.4(ATP6V1A):c.1291-7dup	rs538710134

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