Variants in gene GLB1 with conflicting interpretations "uncertain significance" and "likely benign"

Submission 1 (uncertain significance) minimum review status:		Submission 1 (uncertain significance) method:
Submission 2 (likely benign) minimum review status:		Submission 2 (likely benign) 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: 5

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HGVS	dbSNP	gnomAD frequency
NM_000404.4(GLB1):c.1285C>T (p.Pro429Ser)	rs180869784	0.00116
NM_000404.4(GLB1):c.623G>A (p.Arg208His)	rs111840209	0.00103
NM_000404.4(GLB1):c.1588C>T (p.Arg530Cys)	rs371397760	0.00095
NM_000404.4(GLB1):c.1426C>T (p.Leu476=)	rs113534264	0.00080
NM_000404.4(GLB1):c.2012A>G (p.Asp671Gly)	rs1696330609	0.00001

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