rs8179183
A SNP in the LEPR gene on chromosome 1. Its most notable genotype is C;G: less likely to gain weight if taking risperidone
- Gene
- LEPR
- Location
- Chr 165,610,269 (GRCh38)
- Highest magnitude
- 1.0Minor
- Tested on
- 23andMe, FamilyTreeDNA
- Minor allele frequency
- 15%
Genotypes
As shown in 23andMe and AncestryDNA files.
- C;CNot ratednormal
- C;GMost notableGoodless likely to gain weight if taking risperidone
- G;GGoodless likely to gain weight if taking risperidone
On SNPedia: (C;C), (C;G), (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.
- AverageC;C <1% C;G 19% G;G 81%
- European ancestry (Utah)C;C 2% C;G 17% G;G 82%
- Han Chinese (Beijing)C;C 0% C;G 4% G;G 96%
- Japanese (Tokyo)C;C 0% C;G 25% G;G 75%
- Yoruba (Nigeria)C;C 0% C;G 29% G;G 71%
Related
Conditions, medicines and genes
Notes
From SNPedia
Notes
rs8179183 is a SNP in the leptin receptor LEPR gene. In a study of 101 mostly Caucasian patients prescribed the atypical antipsychotic risperidone, carriers of a rs8179183(G) allele were less likely to gain significant weight compared to rs8179183(C;C) carriers, as assessed by physiogenomic analysis of corresponding weight profiles. Two other SNPs, rs6837793 and rs705381, were also significantly associated with weight profiles in these patients.
Source and license
Adapted from rs8179183 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 Its entries can be incomplete, out of date or wrong, and nothing here is a diagnosis or medical advice.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.