List of variants in gene ATP6V0A2 reported as likely benign by Athena Diagnostics

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_012463.4(ATP6V0A2):c.773A>G (p.Glu258Gly)	rs141467923	0.00087
NM_012463.4(ATP6V0A2):c.2384C>T (p.Ala795Val)	rs139509075	0.00043
NM_012463.4(ATP6V0A2):c.312C>T (p.Leu104=)	rs563333869	0.00004

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