Variants in gene PKP2 with conflicting interpretations "pathogenic" and "uncertain significance"

Submission 1 (pathogenic) minimum review status:		Submission 1 (pathogenic) method:
Submission 2 (uncertain significance) minimum review status:		Submission 2 (uncertain significance) 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: 3

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HGVS	dbSNP	gnomAD frequency
NM_001005242.3(PKP2):c.1379-1998C>T	rs151212477	0.00001
NM_001005242.3(PKP2):c.1379-2047_1379-2043del	rs775995156
NM_001005242.3(PKP2):c.2445+1G>A	rs1060499891

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