List of variants in gene PKP1 reported as likely pathogenic for hereditary epidermal appendage anomaly

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: 2

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HGVS	dbSNP	gnomAD frequency
NM_001005337.3(PKP1):c.203-1G>C	rs2102154917
NM_001005337.3(PKP1):c.841C>T (p.Gln281Ter)	rs1553275192

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