rs2854128(A;A)
G2706A+, probably MT-Haplogroup H.
- Magnitude
- 1.0Minor
- Repute
- Bad
- Frequency
- 11%Average of 4 populations
- On SNPedia
- rs2854128(A;A)
- Gene
- None listed
Frequency
Share of people with A;A in each HapMap population.
- European ancestry (Utah)45%
- Han Chinese (Beijing)0%
- Japanese (Tokyo)0%
- Yoruba (Nigeria)0%
Other genotypes of rs2854128
Notes
From SNPedia
One of the 2 ancestral mitochondrial mutations needed for mitochondrial Haplogroup H. This is a non-synonymous mutation in the mitochondrial ribosome, and possibly in the neuroprotective protein humanin. Haplogroup H has been associated with increased risk of age-related neurological diseases, suggesting that this mutation (or some other) may slightly reduce the effectiveness of mitochondria or humanin.
Source and license
Adapted from rs2854128(A;A) 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.