rs397514043
A SNP in the DSC2 gene on chromosome 18. Its most notable genotype is -;C: Arrhythmogenic right ventricular dysplasia
- Gene
- DSC2
- Location
- Chr 1831,074,730 (GRCh38)
- Highest magnitude
- 6.7Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- -;CMost notableBadArrhythmogenic right ventricular dysplasia
- C;CGoodcommon in clinvar
SNPedia records rs397514043 on the minus strand: (-;G), (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Source and license
Adapted from rs397514043 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.