rs397517005
A SNP in the PKP2 gene on chromosome 12. Its most notable genotype is -;G: Arrhythmogenic right ventricular dysplasia
- Gene
- PKP2
- Location
- Chr 1232,824,142 (GRCh38)
- Highest magnitude
- 6.7Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- -;GMost notableBadArrhythmogenic right ventricular dysplasia
- G;GGoodcommon in clinvar
SNPedia records rs397517005 on the minus strand: (-;C), (C;C). 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 rs397517005 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.