| Literature DB >> 15961272 |
Raymond D Miller1, Michael S Phillips, Inho Jo, Miriam A Donaldson, Joel F Studebaker, Nicholas Addleman, Steven V Alfisi, Wendy M Ankener, Hamid A Bhatti, Chad E Callahan, Benjamin J Carey, Cheryl L Conley, Justin M Cyr, Vram Derohannessian, Rachel A Donaldson, Carolina Elosua, Stacey E Ford, Angela M Forman, Craig A Gelfand, Nicole M Grecco, Susan M Gutendorf, Cricket R Hock, Mark J Hozza, Soyoung Hur, Sun Mi In, Diana L Jackson, Sangmee Ahn Jo, Sung-Chul Jung, Sook Kim, Kuchan Kimm, Ellen F Kloss, Daniel C Koboldt, Jennifer M Kuebler, Feng-Shen Kuo, Jessica A Lathrop, Jong-Keuk Lee, Kathy L Leis, Stephanie A Livingston, Elizabeth G Lovins, Maria L Lundy, Sima Maggan, Matthew Minton, Michael A Mockler, David W Morris, Eric P Nachtman, Bermseok Oh, Chan Park, Chang-Wook Park, Nicholas Pavelka, Adrienne B Perkins, Stephanie L Restine, Ravi Sachidanandam, Andrew J Reinhart, Kathryn E Scott, Gira J Shah, Jatana M Tate, Shobha A Varde, Amy Walters, J Rebecca White, Yeon-Kyeong Yoo, Jong-Eun Lee, Michael T Boyce-Jacino, Pui-Yan Kwok.
Abstract
Here we report a large, extensively characterized set of single-nucleotide polymorphisms (SNPs) covering the human genome. We determined the allele frequencies of 55,018 SNPs in African Americans, Asians (Japanese-Chinese), and European Americans as part of The SNP Consortium's Allele Frequency Project. A subset of 8333 SNPs was also characterized in Koreans. Because these SNPs were ascertained in the same way, the data set is particularly useful for modeling. Our results document that much genetic variation is shared among populations. For autosomes, some 44% of these SNPs have a minor allele frequency > or =10% in each population, and the average allele frequency differences between populations with different continental origins are less than 19%. However, the several percentage point allele frequency differences among the closely related Korean, Japanese, and Chinese populations suggest caution in using mixtures of well-established populations for case-control genetic studies of complex traits. We estimate that approximately 7% of these SNPs are private SNPs with minor allele frequencies <1%. A useful set of characterized SNPs with large allele frequency differences between populations (>60%) can be used for admixture studies. High-density maps of high-quality, characterized SNPs produced by this project are freely available.Entities:
Mesh:
Year: 2005 PMID: 15961272 PMCID: PMC1885222 DOI: 10.1016/j.ygeno.2005.04.012
Source DB: PubMed Journal: Genomics ISSN: 0888-7543 Impact factor: 5.736