rs397517022
A SNP in the PKP2 gene on chromosome 12. Its most notable genotype is CAGT;TCCTG: Arrhythmogenic right ventricular dysplasia
- Gene
- PKP2
- Location
- Chr 1232,796,260 (GRCh38)
- Highest magnitude
- 6.7Very important
- Tested on
- 23andMe
Genotypes
As shown in 23andMe and AncestryDNA files.
- CAGT;TCCTGMost notableBadArrhythmogenic right ventricular dysplasia
- TCCTG;TCCTGGoodcommon in clinvar
On SNPedia: (CAGT;TCCTG), (TCCTG;TCCTG). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other PKP2 SNPs
- rs78897684C;GArrhythmogenic right ventricular dysplasiaVery important
- rs111517471A;CArrhythmogenic right ventricular dysplasiaVery important
- rs121434420A;GArrhythmogenic right ventricular dysplasiaVery important
- rs121434421A;GArrhythmogenic right ventricular dysplasiaVery important
- rs193922674C;GArrhythmogenic right ventricular dysplasiaVery important
- rs372827156A;GArrhythmogenic right ventricular dysplasiaVery important
- rs397516986A;GArrhythmogenic right ventricular dysplasiaVery important
- rs397516989-;AArrhythmogenic right ventricular dysplasiaVery important
Source and license
Adapted from rs397517022 on SNPedia, using a snapshot taken October 16, 2026. SNPedia content is shared under CC BY-NC-SA 3.0 US, and this page is shared under the same license.
SNPedia is a community-edited wiki. Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice. Magnitude is a community rating of how interesting a genotype is, not a risk score.