Haplotype variation and linkage disequilibrium in 313 human genes
- PMID: 11452081
- DOI: 10.1126/science.1059431
Haplotype variation and linkage disequilibrium in 313 human genes
Erratum in
- Science 2001 Aug 10;293(5532):1048
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.
Similar articles
-
Nucleotide diversity and haplotype structure of the human angiotensinogen gene in two populations.Am J Hum Genet. 2002 Jan;70(1):108-23. doi: 10.1086/338454. Epub 2001 Nov 30. Am J Hum Genet. 2002. PMID: 11731937 Free PMC article.
-
Population differences in DNA sequence variation and linkage disequilibrium at the PON1 gene.Ann Hum Genet. 2004 Mar;68(Pt 2):110-9. doi: 10.1046/j.1529-8817.2003.00077.x. Ann Hum Genet. 2004. PMID: 15008790
-
Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase.Am J Hum Genet. 1998 Aug;63(2):595-612. doi: 10.1086/301977. Am J Hum Genet. 1998. PMID: 9683608 Free PMC article.
-
Comparison of linkage disequilibrium patterns and haplotype structure of eight single nucleotide polymorphisms across the CYP1A2 gene between the Korean, and other populations registered in the International HapMap database.J Clin Pharm Ther. 2009 Aug;34(4):429-36. doi: 10.1111/j.1365-2710.2008.01011.x. J Clin Pharm Ther. 2009. PMID: 19583676
-
Antipsychotic medications and ethnicity.J Gend Specif Med. 1998 Oct-Nov;1(2):16-7. J Gend Specif Med. 1998. PMID: 11281006 Review. No abstract available.
Cited by
-
Advancing genomic research and reducing health disparities: what can nurse scholars do?J Nurs Scholarsh. 2013 Jun;45(2):202-9. doi: 10.1111/j.1547-5069.2012.01482.x. Epub 2013 Mar 1. J Nurs Scholarsh. 2013. PMID: 23452096 Free PMC article.
-
Genetic risk factors for deep vein thrombosis among Japanese: importance of protein S K196E mutation.Int J Hematol. 2006 Apr;83(3):217-23. doi: 10.1532/IJH97.A20514. Int J Hematol. 2006. PMID: 16720551 Review.
-
Genetic sequence variations and ADPRT haplotype analysis in French Canadian families with high risk of breast cancer.J Hum Genet. 2007;52(12):963-977. doi: 10.1007/s10038-007-0203-9. Epub 2007 Oct 18. J Hum Genet. 2007. PMID: 17943227
-
Association mapping with single-feature polymorphisms.Genetics. 2006 Jun;173(2):1125-33. doi: 10.1534/genetics.105.052720. Epub 2006 Mar 1. Genetics. 2006. PMID: 16510789 Free PMC article.
-
Establishment of a pipeline to analyse non-synonymous SNPs in Bos taurus.BMC Genomics. 2006 Nov 26;7:298. doi: 10.1186/1471-2164-7-298. BMC Genomics. 2006. PMID: 17125523 Free PMC article.
Publication types
MeSH terms
Substances
LinkOut - more resources
Full Text Sources
Other Literature Sources