rs11671653
A SNP in the DNM2 gene on chromosome 19. Its most notable genotype is G;G: common in complete genomics
- Gene
- DNM2
- Location
- Chr 1910,727,810 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 8%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (G;G). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageG;G 84%
- European ancestry (Utah)G;G 80%
- Han Chinese (Beijing)G;G 88%
- Japanese (Tokyo)G;G 99%
- Yoruba (Nigeria)G;G 77%
- African ancestry (Southwest US)G;G 84%
- Chinese (Denver)G;G 90%
- Gujarati IndianG;G 84%
- Luhya (Kenya)G;G 69%
- Mexican ancestry (Los Angeles)G;G 93%
- Maasai (Kenya)G;G 78%
- TuscanG;G 83%
Related
Other DNM2 SNPs
- rs121909089A;GDNM2-related intermediate Charcot-Marie-Tooth neuropathyVery important
- rs121909090C;TDNM2-related intermediate Charcot-Marie-Tooth neuropathyVery important
- rs121909091C;TDNM2-related intermediate Charcot-Marie-Tooth neuropathyVery important
- rs121909092A;GDNM2-related intermediate Charcot-Marie-Tooth neuropathyVery important
- rs121909093A;GDNM2-related intermediate Charcot-Marie-Tooth neuropathyVery important
- rs587783594A;TDNM2-related intermediate Charcot-Marie-Tooth neuropathyVery important
- rs587783595A;GDNM2-related intermediate Charcot-Marie-Tooth neuropathyVery important
- rs587783597C;TDNM2-related intermediate Charcot-Marie-Tooth neuropathyVery important
Source and license
Adapted from rs11671653 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.