rs398122853
A SNP in the DMD gene on chromosome X. Its most notable genotype is T;T: Dilated cardiomyopathy
- Gene
- DMD
- Location
- Chr X33,211,304 (GRCh38)
- Highest magnitude
- 6.2Very important
- Tested on
- AncestryDNA
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
- T;TMost notableBadDilated cardiomyopathy
- C;TBadDilated cardiomyopathy
- C;CGoodcommon in clinvar
SNPedia records rs398122853 on the minus strand: (A;A), (A;G), (G;G). 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
- rs373286166C;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 rs398122853 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.