List of variants in gene PKP2 reported as uncertain significance by Center for Genomics, Ann and Robert H. Lurie Children's Hospital of Chicago

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_001005242.3(PKP2):c.1379-2109G>A	rs139159464	0.00050
NM_001005242.3(PKP2):c.184C>A (p.Gln62Lys)	rs199601548	0.00020
NM_001005242.3(PKP2):c.224-3C>G	rs786204387

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