Variant (rsID / SNP)

rs768286281

rs768286281 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKP2. Location: chromosome 12, position 32,975,529. Clinical significance in the table: Conflicting interpretations of pathogenicity.

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Reference-table entries

PKP2Conflicting interpretations

Clinical significance (as recorded): Conflicting interpretations of pathogenicity
Variant type: single nucleotide variant
Chromosome / position: 12:32975529
Cytoband: 12p11.21
HGVS: NM_001005242.3(PKP2):c.1711T>A (p.Ser571Thr)
Allele change: Missense_S571T

Associated conditions / phenotypes

Arrhythmogenic right ventricular dysplasia 9

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.