rs397516712
A SNP in the DSG2 gene on chromosome 18. Its most notable genotype is A;C: Arrhythmogenic right ventricular dysplasia
- Gene
- DSG2
- Location
- Chr 1831,524,815 (GRCh38)
- Highest magnitude
- 6.7Very important
- Tested on
- 23andMe, AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- A;CMost notableBadArrhythmogenic right ventricular dysplasia
- C;CGoodcommon in clinvar
On SNPedia: (A;C), (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other DSG2 SNPs
- rs121913007A;GArrhythmogenic right ventricular dysplasiaVery important
- rs121913008A;GArrhythmogenic right ventricular dysplasiaVery important
- rs121913009A;GArrhythmogenic right ventricular dysplasiaVery important
- rs121913011A;GArrhythmogenic right ventricular dysplasiaVery important
- rs397516703-;TGArrhythmogenic right ventricular dysplasiaVery important
- rs553299589A;GArrhythmogenic right ventricular dysplasiaVery important
- rs750176752A;GArrhythmogenic right ventricular dysplasiaVery important
- rs794728086C;TArrhythmogenic right ventricular dysplasiaVery important
Source and license
Adapted from rs397516712 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.