ClinVar Miner

Variants in gene combination C10orf105, CDH23 with conflicting interpretations reported as "benign and "pathogenic"

Submission 1 (benign) minimum review status:		Submission 1 (benign) method:
Submission 2 (pathogenic) minimum review status:		Submission 2 (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: 1

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HGVS	dbSNP	gnomAD frequency
NM_022124.6(CDH23):c.4104+15del	rs1839422034

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