Variants associated with common disease are not unusually differentiated in frequency across populations
- PMID: 16385456
- PMCID: PMC1380210
- DOI: 10.1086/499287
Variants associated with common disease are not unusually differentiated in frequency across populations
Abstract
Genetic variants that contribute to risk of common disease may differ in frequency across populations more than random variants in the genome do, perhaps because they have been exposed to population-specific natural selection. To assess this hypothesis empirically, we analyzed data from two groups of single-nucleotide polymorphisms (SNPs) that have shown reproducible (n = 9) or reported (n = 39) associations with common diseases. We compared the frequency differentiation (between Europeans and Africans) of the disease-associated SNPs with that of random SNPs in the genome. These common-disease-associated SNPs are not significantly more differentiated across populations than random SNPs. Thus, for the data examined here, ethnicity will not be a good predictor of genotype at many common-disease-associated SNPs, just as it is rarely a good predictor of genotype at random SNPs in the genome.
References
Web Resources
- 
    - HapMap Project, http://www.hapmap.org/
 
- 
    - Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/Omim/
 
- 
    - Seattle SNPs, http://pga.gs.washington.edu/ (for National Heart, Lung, and Blood Institute Program for Genomic Application, Seattle SNPs, Seattle, WA [July 2004])
 
References
- 
    - Altshuler D, Hirschhorn JN, Klannemark M, Lindgren CM, Vohl MC, Nemesh J, Lane CR, Schaffner SF, Bolk S, Brewer C, Tuomi T, Gaudet D, Hudson TJ, Daly M, Groop L, Lander ES (2000) The common PPARγ Pro12Ala polymorphism is associated with decreased risk of type 2 diabetes. Nat Genet 26:76–8010.1038/79216 - DOI - PubMed
 
Publication types
MeSH terms
LinkOut - more resources
- Full Text Sources
- Medical
 
        