Variants in gene ATP6V1B1 with conflicting interpretations "pathogenic" and "likely pathogenic"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (likely pathogenic) minimum review status:		Submission 2 (likely pathogenic) method:
Gene type: Distinguish antisense genes from sense genes
Show significances as they were submitted (without aggregation into standard terms)
		ClinVar version:

Total variants with conflicting interpretations: 4

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HGVS	dbSNP	gnomAD frequency
NM_001692.4(ATP6V1B1):c.232G>A (p.Gly78Arg)	rs121964881	0.00009
NM_001692.4(ATP6V1B1):c.943C>T (p.Arg315Ter)	rs145536062	0.00004
NM_001692.4(ATP6V1B1):c.27_28delinsC (p.Leu12fs)	rs1679840658
NM_001692.4(ATP6V1B1):c.484G>T (p.Glu162Ter)	rs1553419751

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