rs28358286
A SNP in the ND4 gene on chromosome MT. Its most notable genotype is C;C.
- Gene
- ND4
- Location
- Chr MT11,674 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe
- Minor allele frequency
- 1%
Genotypes
As shown in 23andMe and AncestryDNA files.
On SNPedia: (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.
- AverageC;C 99%
- European ancestry (Utah)C;C 97%
- Han Chinese (Beijing)C;C 100%
- Japanese (Tokyo)C;C 100%
- Yoruba (Nigeria)C;C 100%
Related
Other ND4 SNPs
- rs199476112A;ALeber's Optic AtrophyVery important
- rs2853493G;GA11467G+, MT-Haplogroup U or KMinor
- rs2853496G;Gcommon genotypeTypical
- rs2853497G;GNo summary available.Typical
- rs2857284C;CNo summary available.Typical
- rs2857285T;TNo summary available.Typical
- rs28358285T;TNo summary available.Typical
- rs28359168A;ANo summary available.Typical
Source and license
Adapted from rs28358286 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.