Ubiquitous Polygenicity of Human Complex Traits: Genome-Wide Analysis of 49 Traits in Koreans

Recent studies in population of European ancestry have shown that 30%∼50% of heritability for human complex traits such as height and body mass index, and common diseases such as schizophrenia and rheumatoid arthritis, can be captured by common SNPs and that genetic variation attributed to chromosom...

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Main Authors: Yang, Jian, Lee, Taeheon, Kim, Jaemin, Cho, Myeong-Chan, Han, Bok-Ghee, Lee, Jong-Young, Lee, Hyun-Jeong, Cho, Seoae, Kim, Heebal
Format: Online
Language:English
Published: Public Library of Science 2013
Online Access:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591292/
id pubmed-3591292
recordtype oai_dc
spelling pubmed-35912922013-03-15 Ubiquitous Polygenicity of Human Complex Traits: Genome-Wide Analysis of 49 Traits in Koreans Yang, Jian Lee, Taeheon Kim, Jaemin Cho, Myeong-Chan Han, Bok-Ghee Lee, Jong-Young Lee, Hyun-Jeong Cho, Seoae Kim, Heebal Research Article Recent studies in population of European ancestry have shown that 30%∼50% of heritability for human complex traits such as height and body mass index, and common diseases such as schizophrenia and rheumatoid arthritis, can be captured by common SNPs and that genetic variation attributed to chromosomes are in proportion to their length. Using genome-wide estimation and partitioning approaches, we analysed 49 human quantitative traits, many of which are relevant to human diseases, in 7,170 unrelated Korean individuals genotyped on 326,262 SNPs. For 43 of the 49 traits, we estimated a nominally significant (P<0.05) proportion of variance explained by all SNPs on the Affymetrix 5.0 genotyping array (). On average across 47 of the 49 traits for which the estimate of is non-zero, common SNPs explain approximately one-third (range of 7.8% to 76.8%) of narrow sense heritability. Public Library of Science 2013-03-07 /pmc/articles/PMC3591292/ /pubmed/23505390 http://dx.doi.org/10.1371/journal.pgen.1003355 Text en © 2013 Yang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
repository_type Open Access Journal
institution_category Foreign Institution
institution US National Center for Biotechnology Information
building NCBI PubMed
collection Online Access
language English
format Online
author Yang, Jian
Lee, Taeheon
Kim, Jaemin
Cho, Myeong-Chan
Han, Bok-Ghee
Lee, Jong-Young
Lee, Hyun-Jeong
Cho, Seoae
Kim, Heebal
spellingShingle Yang, Jian
Lee, Taeheon
Kim, Jaemin
Cho, Myeong-Chan
Han, Bok-Ghee
Lee, Jong-Young
Lee, Hyun-Jeong
Cho, Seoae
Kim, Heebal
Ubiquitous Polygenicity of Human Complex Traits: Genome-Wide Analysis of 49 Traits in Koreans
author_facet Yang, Jian
Lee, Taeheon
Kim, Jaemin
Cho, Myeong-Chan
Han, Bok-Ghee
Lee, Jong-Young
Lee, Hyun-Jeong
Cho, Seoae
Kim, Heebal
author_sort Yang, Jian
title Ubiquitous Polygenicity of Human Complex Traits: Genome-Wide Analysis of 49 Traits in Koreans
title_short Ubiquitous Polygenicity of Human Complex Traits: Genome-Wide Analysis of 49 Traits in Koreans
title_full Ubiquitous Polygenicity of Human Complex Traits: Genome-Wide Analysis of 49 Traits in Koreans
title_fullStr Ubiquitous Polygenicity of Human Complex Traits: Genome-Wide Analysis of 49 Traits in Koreans
title_full_unstemmed Ubiquitous Polygenicity of Human Complex Traits: Genome-Wide Analysis of 49 Traits in Koreans
title_sort ubiquitous polygenicity of human complex traits: genome-wide analysis of 49 traits in koreans
description Recent studies in population of European ancestry have shown that 30%∼50% of heritability for human complex traits such as height and body mass index, and common diseases such as schizophrenia and rheumatoid arthritis, can be captured by common SNPs and that genetic variation attributed to chromosomes are in proportion to their length. Using genome-wide estimation and partitioning approaches, we analysed 49 human quantitative traits, many of which are relevant to human diseases, in 7,170 unrelated Korean individuals genotyped on 326,262 SNPs. For 43 of the 49 traits, we estimated a nominally significant (P<0.05) proportion of variance explained by all SNPs on the Affymetrix 5.0 genotyping array (). On average across 47 of the 49 traits for which the estimate of is non-zero, common SNPs explain approximately one-third (range of 7.8% to 76.8%) of narrow sense heritability.
publisher Public Library of Science
publishDate 2013
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3591292/
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