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The design and interpretation of genetic association studies depends on the relationship between the genotyped variants and the underlying functional variant, often parameterized as the squared correlation or r(2) measure of linkage disequilibrium between two loci. While it has long been recognized that placing a constraint on ther(2) between two loci also places a constraint on the difference in frequencies between the coupled alleles, this constraint has not been quantified. Here, quantification of this severe constraint is presented. For example, for r(2) >/= .8, the maximum difference in allele frequency is +/- .06 which occurs when one locus has allele frequency .5. For r(2) >/= .8 and allele frequency at one locus of .1, the maximum difference in allele frequency at the second locus is only +/- .02. The impact on the design and interpretation of association studies is discussed.

Original publication

DOI

10.1375/1832427053738827

Type

Journal article

Journal

Twin Res Hum Genet

Publication Date

04/2005

Volume

8

Pages

87 - 94

Keywords

Algorithms, Chromosome Mapping, Data Interpretation, Statistical, Gene Frequency, Genetic Markers, Genetic Variation, Genotype, Humans, Linkage Disequilibrium, Polymorphism, Single Nucleotide, Research Design