Literature DB >> 12768436

Characterization of 458 single nucleotide polymorphisms of disease candidate genes in the Korean population.

Jong-Keuk Lee1, Hung-Tae Kim1, Sung-Mi Cho1, Kyung-Hee Kim1, Hee-Jeong Jin1, Gil-Mi Ryu1, Bermseok Oh1, Chan Park1, Kuchan Kimm1, Sangmee Ahn Jo2, Sung-Chul Jung2, Sook Kim3, Sun Mi In3, Jong-Eun Lee3, Inho Jo4.   

Abstract

Single nucleotide polymorphisms (SNPs) are considered as very promising genetic markers for complex disease gene hunting. However, it has been demonstrated that there are significant ethnic differences in genetic variations. In order to investigate the genetic variations in the Korean population and their ethnic differences, a large number of SNPs of 161 disease candidate genes were collected from a publicly available SNP database and then tested for the distribution of allele frequency in the Korean population. Of all 458 SNPs tested, approximately 43.9% were polymorphic in the Korean population, whereas 44.5% were monomorphic. The remaining 11.6% were failed in the test. Significant differences have been observed when SNP allele frequency pattern of Koreans was compared with those of Caucasians and Africans, whereas this pattern was highly similar between Korean and Japanese populations. Our data indicate that although many of the SNPs available in publicly available database, especially coding-region SNPs (cSNPs), can be used as informative genetic markers for disease association studies, an extensive verification of public SNPs in a particular population studied should be undertaken prior to their association studies.

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Year:  2003        PMID: 12768436     DOI: 10.1007/s10038-003-0011-9

Source DB:  PubMed          Journal:  J Hum Genet        ISSN: 1434-5161            Impact factor:   3.172


  9 in total

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Journal:  Nat Genet       Date:  1999-07       Impact factor: 38.330

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Authors:  G C Johnson; J A Todd
Journal:  Curr Opin Genet Dev       Date:  2000-06       Impact factor: 5.578

6.  Gene-based SNP discovery as part of the Japanese Millennium Genome Project: identification of 190,562 genetic variations in the human genome. Single-nucleotide polymorphism.

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Journal:  J Hum Genet       Date:  2002       Impact factor: 3.172

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Journal:  Nat Genet       Date:  2000-10       Impact factor: 38.330

  9 in total
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  6 in total

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