rs2168889
A SNP on chromosome 4. Its most notable genotype is A;A: common genotype
- Gene
- None listed
- Location
- Chr 474,357,994 (GRCh38)
- Highest magnitude
- 0.0Typical
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 5%
Genotypes
Plus strand, as in 23andMe and AncestryDNA files.
SNPedia records rs2168889 on the minus strand: (T;T). 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 89%
- European ancestry (Utah)A;A 89%
- Han Chinese (Beijing)A;A 91%
- Japanese (Tokyo)A;A 86%
- Yoruba (Nigeria)A;A 91%
Source and license
Adapted from rs2168889 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.