Variant (rsID / SNP)
rs144601090
rs144601090 is a genetic variant (SNP, identifier in the dbSNP catalogue) that the reference table assigns to PKP2. Location: chromosome 12, position 32,974,373. Clinical significance in the table: Conflicting interpretations of pathogenicity.
Reference-table entries
PKP2Conflicting interpretations
- Clinical significance (as recorded)
- Conflicting interpretations of pathogenicity
- Variant type
- single nucleotide variant
- Chromosome / position
- 12:32974373
- Cytoband
- 12p11.21
- HGVS
- NM_001005242.3(PKP2):c.1930T>C (p.Ser644Pro)
- Allele change
- Missense_S644P
Associated conditions / phenotypes
Arrhythmogenic right ventricular cardiomyopathy|Arrhythmogenic right ventricular dysplasia 9|Cardiovascular phenotype|Cardiomyopathy
Public references
Classifications are reproduced unchanged from the reference table. For education only; not a substitute for medical or genetic counselling.