Genome-wide compound heterozygote analysis highlights alleles associated with adult height in Europeans View Full Text


Ontology type: schema:ScholarlyArticle      Open Access: True


Article Info

DATE

2017-11

AUTHORS

Kaiyin Zhong, Gu Zhu, Xiaoxi Jing, A. Emile J. Hendriks, Sten L. S. Drop, M. Arfan Ikram, Scott Gordon, Changqing Zeng, Andre G. Uitterlinden, Nicholas G. Martin, Fan Liu, Manfred Kayser

ABSTRACT

Adult height is the most widely genetically studied common trait in humans; however, the trait variance explainable by currently known height-associated single nucleotide polymorphisms (SNPs) identified from the previous genome-wide association studies (GWAS) is yet far from complete given the high heritability of this complex trait. To exam if compound heterozygotes (CH) may explain extra height variance, we conducted a genome-wide analysis to screen for CH in association with adult height in 10,631 Dutch Europeans enriched with extremely tall people, using our recently developed method implemented in the software package CollapsABEL. The analysis identified six regions (3q23, 5q35.1, 6p21.31, 6p21.33, 7q21.2, and 9p24.3), where multiple pairs of SNPs as CH showed genome-wide significant association with height (P < 1.67 × 10-10). Of those, 9p24.3 represents a novel region influencing adult height, whereas the others have been highlighted in the previous GWAS on height based on analysis of individual SNPs. A replication analysis in 4080 Australians of European ancestry confirmed the significant CH-like association at 9p24.3 (P < 0.05). Together, the collapsed genotypes at these six loci explained 2.51% of the height variance (after adjusting for sex and age), compared with 3.23% explained by the 14 top-associated SNPs at 14 loci identified by traditional GWAS in the same data set (P < 5 × 10-8). Overall, our study empirically demonstrates that CH plays an important role in adult height and may explain a proportion of its "missing heritability". Moreover, our findings raise promising expectations for other highly polygenic complex traits to explain missing heritability identifiable through CH-like associations. More... »

PAGES

1407-1417

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  • Identifiers

    URI

    http://scigraph.springernature.com/pub.10.1007/s00439-017-1842-3

    DOI

    http://dx.doi.org/10.1007/s00439-017-1842-3

    DIMENSIONS

    https://app.dimensions.ai/details/publication/pub.1091830915

    PUBMED

    https://www.ncbi.nlm.nih.gov/pubmed/28921393


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