Variant (rsID / SNP)

rs786204388

rs786204388 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKP2. Location: chromosome 12, position 33,031,934. Clinical significance in the table: Pathogenic/Likely pathogenic.

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Reference-table entries

PKP2Pathogenic

Clinical significance (as recorded): Pathogenic/Likely pathogenic
Variant type: Deletion
Chromosome / position: 12:33031934
Cytoband: 12p11.21
HGVS: NM_001005242.3(PKP2):c.253_256del (p.Glu85fs)

Associated conditions / phenotypes

Sudden unexplained death|Arrhythmogenic right ventricular dysplasia 9|Cardiomyopathy

Public references

dbSNP
ClinVar
Ensembl
gnomAD

Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.