Haplotype variation and haplotype linkage disequilibrium in 313 human genes

732Citations
Citations of this article
312Readers
Mendeley users who have this article in their library.
Get full text

Abstract

Variation within genes has important implications for all biological traits. We identified 3899 single nucleotide polymorphisms (SNPs) that were present within 313 genes from 82 unrelated individuals of diverse ancestry, and we organized the SNPs into 4304 different haplotypes. Each gene had several variable SNPs and haplotypes that were present in all populations, as well as a number that were population-specific. Pairs of SNPs exhibited variability in the degree of linkage disequilibrium that was a function of their location within a gene, distance from each other, population distribution, and population frequency. Haplotypes generally had more information content (heterozygosity) than did individual SNPs. Our analysis of the pattern of variation strongly supports the recent expansion of the human population.

Cite

CITATION STYLE

APA

Stephens, J. C., Schneider, J. A., Tanguay, D. A., Choi, J., Acharya, T., Stanley, S. E., … Vovis, G. F. (2001). Haplotype variation and haplotype linkage disequilibrium in 313 human genes. Science, 293(5529), 489–493. https://doi.org/10.1126/science.1059431

Register to see more suggestions

Mendeley helps you to discover research relevant for your work.

Already have an account?

Save time finding and organizing research with Mendeley

Sign up for free