rs1064325
A SNP in the DMD gene on chromosome X. Its most notable genotype is G;G: common in clinvar
- Gene
- DMD
- Location
- Chr X32,345,999 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- Not on consumer chips
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs1064325 on the minus strand: (C;C). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 4 HapMap populations.
- AverageG;G 100%
- European ancestry (Utah)G;G 100%
- Han Chinese (Beijing)G;G 100%
- Japanese (Tokyo)G;G 100%
- Yoruba (Nigeria)G;G 100%
Related
Other DMD SNPs
- rs104894797A;GDilated cardiomyopathyVery important
- rs128627256A;GDilated cardiomyopathyVery important
- rs373286166C;TDilated cardiomyopathyVery important
- rs398122853T;TDilated cardiomyopathyVery important
- rs398123832A;GDilated cardiomyopathyVery important
- rs398123909A;CDilated cardiomyopathyVery important
- rs398123923A;CDilated cardiomyopathyVery important
- rs794726993A;GDilated cardiomyopathyVery important
Source and license
Adapted from rs1064325 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.