rs373286166
A SNP in the DMD gene on chromosome X. Its most notable genotype is C;T: Dilated cardiomyopathy
- Gene
- DMD
- Location
- Chr X32,573,529 (GRCh38)
- Highest magnitude
- 6.2Very important
- Tested on
- AncestryDNA
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CGoodcommon in clinvar
- C;TMost notableBadDilated cardiomyopathy
- T;TBadDilated cardiomyopathy
On SNPedia: (C;C), (C;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Related
Other DMD SNPs
- rs104894797A;GDilated cardiomyopathyVery important
- rs128627256A;GDilated cardiomyopathyVery important
- rs398122853T;TDilated cardiomyopathyVery important
- rs398123832A;GDilated cardiomyopathyVery important
- rs398123909A;CDilated cardiomyopathyVery important
- rs398123923A;CDilated cardiomyopathyVery important
- rs794726993A;GDilated cardiomyopathyVery important
- rs1800278C;CNo summary available.Typical
Source and license
Adapted from rs373286166 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.