rs4489954
A SNP in the MAP2K5 gene on chromosome 15. Its most notable genotype is T;T: >0.69x risk of developing restless legs syndrome
- Gene
- MAP2K5
- Location
- Chr 1567,779,737 (GRCh38)
- Highest magnitude
- 1.8Minor
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 46%
Genotypes
As shown in 23andMe and AncestryDNA files.
- G;GBadNormal risk of developing restless legs syndrome
- G;TGood0.69x risk risk of developing restless legs syndrome
- T;TMost notableGood>0.69x risk of developing restless legs syndrome
On SNPedia: (G;G), (G;T), (T;T). Magnitude rates how notable a genotype is from 0 to 10, not how risky it is.
Frequency
Share of each genotype in 11 HapMap populations.
- AverageG;G 30% G;T 45% T;T 25%
- European ancestry (Utah)G;G 50% G;T 46% T;T 5%
- Han Chinese (Beijing)G;G 7% G;T 46% T;T 47%
- Japanese (Tokyo)G;G 10% G;T 42% T;T 49%
- Yoruba (Nigeria)G;G 35% G;T 54% T;T 11%
- African ancestry (Southwest US)G;G 37% G;T 51% T;T 12%
- Chinese (Denver)G;G 10% G;T 40% T;T 50%
- Gujarati IndianG;G 28% G;T 45% T;T 28%
- Luhya (Kenya)G;G 51% G;T 39% T;T 10%
- Mexican ancestry (Los Angeles)G;G 14% G;T 48% T;T 38%
- Maasai (Kenya)G;G 42% G;T 46% T;T 12%
- TuscanG;G 48% G;T 39% T;T 13%
Related
Conditions, medicines and genes
Other MAP2K5 SNPs
Notes
From SNPedia
Notes
rs4489954, a SNP located in a region of chromosome 15q, has been linked to a lower frequency of restless legs syndrome, a common sleep disorder, with an overall odds ratio of 0.69 (CI: 0.69-0.82) for the (T) minor allele.
T;T
But no replication despite being several years since this was first reported
Source and license
Adapted from rs4489954 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.