rs2853493
A SNP in the ND4 gene on chromosome MT. Its most notable genotype is G;G: A11467G+, MT-Haplogroup U or K
- Gene
- ND4
- Location
- Chr MT11,467 (GRCh38)
- Highest magnitude
- 1.0Minor
- Tested on
- 23andMe, AncestryDNA
- Minor allele frequency
- 10%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (A;A), (G;G). 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.
- AverageA;A 94% G;G 6%
- European ancestry (Utah)A;A 75% G;G 25%
- Han Chinese (Beijing)A;A 100% G;G 0%
- Japanese (Tokyo)A;A 100% G;G 0%
- Yoruba (Nigeria)A;A 100% G;G 0%
Related
Other ND4 SNPs
- rs199476112A;ALeber's Optic AtrophyVery important
- rs2853496G;Gcommon genotypeTypical
- rs2853497G;GNo summary available.Typical
- rs2857284C;CNo summary available.Typical
- rs2857285T;TNo summary available.Typical
- rs28358285T;TNo summary available.Typical
- rs28358286C;CNo summary available.Typical
- rs28359168A;ANo summary available.Typical
Genosets
Genosets combine several genotypes. Twofold checks them in your report.
Notes
From SNPedia
Notes
More commonly known as A11467G, or 11467. One of 3 Mitochondrial mutations that together define Mitochondrial Haplogroup U, and its descendants. This is a synonymous change that still codes for the exact same amino acid, so it probably has no biological effect.
A;A
Normal version of A11467G. Not mitochondrial Haplogroup U or K.
G;G
Probably Mitochondrial Haplogroup U or K. Harmless mitochondrial mutation of A11467G.
Source and license
Adapted from rs2853493 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.