Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Comparative Study
. 2006 Jan;78(1):130-6.
doi: 10.1086/499287. Epub 2005 Nov 16.

Variants associated with common disease are not unusually differentiated in frequency across populations

Affiliations
Comparative Study

Variants associated with common disease are not unusually differentiated in frequency across populations

Kirk E Lohmueller et al. Am J Hum Genet. 2006 Jan.

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.

PubMed Disclaimer

References

Web Resources

    1. dbSNP, http://www.ncbi.nlm.nih.gov/SNP/
    1. HapMap Project, http://www.hapmap.org/
    1. Online Mendelian Inheritance in Man (OMIM), http://www.ncbi.nlm.nih.gov/Omim/
    1. PubMed, http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
    1. 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

    1. Aitman TJ, Cooper LD, Norsworthy PJ, Wahid FN, Gray JK, Curtis BR, McKeigue PM, Kwiatkowski D, Greenwood BM, Snow RW, Hill AV, Scott J (2000) Malaria susceptibility and CD36 mutation. Nature 405:1015–101610.1038/35016636 - DOI - PubMed
    1. Akey JM, Zhang G, Zhang K, Jin L, Shriver MD (2002) Interrogating a high-density SNP map for signatures of natural selection. Genome Res 12:1805–181410.1101/gr.631202 - DOI - PMC - PubMed
    1. Allebrandt KV, Souza RL, Chautard-Freire-Maia EA (2002) Variability of the paraoxonase gene (PON1) in Euro- and Afro-Brazilians. Toxicol Appl Pharmacol 180:151–15610.1006/taap.2002.9368 - DOI - PubMed
    1. 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
    1. Bamshad M, Wooding S, Salisbury BA, Stephens JC (2004) Deconstructing the relationship between genetics and race. Nat Rev Genet 5:598–60910.1038/nrg1401 - DOI - PubMed

Publication types