List of variants in gene ATP6V1B2 reported as uncertain significance for Zimmermann-Laband syndrome

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_001693.4(ATP6V1B2):c.1018C>T (p.Arg340Ter)	rs2072836775
NM_001693.4(ATP6V1B2):c.1241A>T (p.Asp414Val)
NM_001693.4(ATP6V1B2):c.1437T>G (p.Ile479Met)	rs2072895089

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