| G2706A+, probably MT-Haplogroup H. |
| Geno
|
Mag
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Summary
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| (A;A)
|
1
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G2706A+, probably MT-Haplogroup H.
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| (G;G)
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0.1
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G2706A-, not MT-Haplogroup H
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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.
