The patterns of natural variation in human genes

被引:80
作者
Crawford, DC [1 ]
Akey, DT [1 ]
Nickerson, DA [1 ]
机构
[1] Univ Washington, Dept Genome Sci, Seattle, WA 98195 USA
关键词
SNPs; haplotypes; diversity; association; linkage disequilibrium; Environmental Genome Project; SeattleSNPs Program for Genomic Applications;
D O I
10.1146/annurev.genom.6.080604.162309
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Currently, more than 10 million DNA sequence variations have been uncovered in the human genome. The most detailed variation discovery efforts have focused on candidate genes involved in cardiovascular disease or in susceptibilities associated with exposure to environmental agents. Here we provide an overview of natural genetic variation from the literature and in 510 human candidate genes resequenced for variation discovery. The average human gene contains 126 biallelic polymorphisms, 46 of which are common (>= 5% minor allele frequency) and 5 of which are found in coding regions. Using this complete picture of genetic diversity, we explore conservation, signatures of selection, and historical recombination to mine information useful for candidate gene association studies. In general, we find that the patterns of human gene variation suggest that no one approach will be appropriate for genetic association studies across all genes. Therefore, many different approaches may be required to identify the elusive genotypes associated with common human phenotypes.
引用
收藏
页码:287 / 312
页数:32
相关论文
共 118 条
  • [11] Listening to silence and understanding nonsense: Exonic mutations that affect splicing
    Cartegni, L
    Chew, SL
    Krainer, AR
    [J]. NATURE REVIEWS GENETICS, 2002, 3 (04) : 285 - 298
  • [12] ESEfinder: a web resource to identify exonic splicing enhancers
    Cartegni, L
    Wang, JH
    Zhu, ZW
    Zhang, MQ
    Krainer, AR
    [J]. NUCLEIC ACIDS RESEARCH, 2003, 31 (13) : 3568 - 3571
  • [13] ADMIXTURE AS A TOOL FOR FINDING LINKED GENES AND DETECTING THAT DIFFERENCE FROM ALLELIC ASSOCIATION BETWEEN LOCI
    CHAKRABORTY, R
    WEISS, KM
    [J]. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1988, 85 (23) : 9119 - 9123
  • [14] Population genetics - making sense out of sequence
    Chakravarti, A
    [J]. NATURE GENETICS, 1999, 21 (Suppl 1) : 56 - 60
  • [15] Predicting the functional consequences of non-synonymous single nucleotide polymorphisms: Structure-based assessment of amino acid variation
    Chasman, D
    Adams, RM
    [J]. JOURNAL OF MOLECULAR BIOLOGY, 2001, 307 (02) : 683 - 706
  • [16] Linkage disequilibrium and inference of ancestral recombination in 538 single-nucleotide polymorphism clusters across the human genome
    Clark, AG
    Nielsen, R
    Signorovitch, J
    Matise, TC
    Glanowski, S
    Heil, J
    Winn-Deen, ES
    Holden, AL
    Lai, E
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 2003, 73 (02) : 285 - 300
  • [17] Haplotype structure and population genetic inferences from nucleotide-sequence variation in human lipoprotein lipase
    Clark, AG
    Weiss, KM
    Nickerson, DA
    Taylor, SL
    Buchanan, A
    Stengård, J
    Salomaa, V
    Vartiainen, E
    Perola, M
    Boerwinkle, E
    Sing, CF
    [J]. AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (02) : 595 - 612
  • [18] Large-scale analysis of non-synonymous coding region single nucleotide polymorphisms
    Clifford, RJ
    Edmonson, MN
    Nguyen, C
    Buetow, KH
    [J]. BIOINFORMATICS, 2004, 20 (07) : 1006 - 1014
  • [19] Multiple rare Alleles contribute to low plasma levels of HDL cholesterol
    Cohen, JC
    Kiss, RS
    Pertsemlidis, A
    Marcel, YL
    McPherson, R
    Hobbs, HH
    [J]. SCIENCE, 2004, 305 (5685) : 869 - 872
  • [20] Finishing the euchromatic sequence of the human genome
    Collins, FS
    Lander, ES
    Rogers, J
    Waterston, RH
    [J]. NATURE, 2004, 431 (7011) : 931 - 945