rs3784709
A SNP in the MAP2K5 gene on chromosome 15. Its most notable genotype is T;T: >0.71x risk of developing restless legs syndrome
- Gene
- MAP2K5
- Location
- Chr 1567,779,937 (GRCh38)
- Highest magnitude
- 1.8Minor
- Tested on
- 23andMe, AncestryDNA, FamilyTreeDNA
- Minor allele frequency
- 47%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CBadNormal risk of developing restless legs syndrome
- C;TGood0.71x risk of developing restless legs syndrome
- T;TMost notableGood>0.71x risk of developing restless legs syndrome
On SNPedia: (C;C), (C;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.
- AverageC;C 31% C;T 44% T;T 25%
- European ancestry (Utah)C;C 47% C;T 48% T;T 5%
- Han Chinese (Beijing)C;C 7% C;T 46% T;T 47%
- Japanese (Tokyo)C;C 10% C;T 45% T;T 45%
- Yoruba (Nigeria)C;C 37% C;T 51% T;T 12%
- African ancestry (Southwest US)C;C 42% C;T 40% T;T 18%
- Chinese (Denver)C;C 10% C;T 40% T;T 50%
- Gujarati IndianC;C 31% C;T 44% T;T 26%
- Luhya (Kenya)C;C 48% C;T 37% T;T 15%
- Mexican ancestry (Los Angeles)C;C 14% C;T 47% T;T 40%
- Maasai (Kenya)C;C 51% C;T 41% T;T 8%
- TuscanC;C 46% C;T 41% T;T 13%
Related
Conditions, medicines and genes
Other MAP2K5 SNPs
Notes
From SNPedia
Notes
rs3784709, 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 0.71 (CI: 0.60-0.83) for the (T) minor allele.
T;T
But no replication despite being several years since this was first reported
Source and license
Adapted from rs3784709 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.