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Attributing the similarity between individuals to genetic and non-genetic factors is central to genetic analyses. In this paper we use the genomic relationship ([Formula: see text]) among 417,060 individuals to investigate the phenotypic covariance between pairs of individuals for 32 traits across the spectrum of relatedness, from unrelated pairs through to identical twins. We find linear relationships between phenotypic covariance and [Formula: see text] that agree with the SNP-based heritability ([Formula: see text]) in unrelated pairs ([Formula: see text]), and with pedigree-estimated heritability in close relatives ([Formula: see text]). The covariance increases faster than [Formula: see text] in distant relatives ([Formula: see text]), and we attribute this to imperfect linkage disequilibrium between causal variants and the common variants used to construct [Formula: see text]. We also examine the effect of assortative mating on heritability estimates from different experimental designs. We find that full-sib identity-by-descent regression estimates for height (0.66 s.e. 0.07) are consistent with estimates from close relatives (0.82 s.e. 0.04) after accounting for the effect of assortative mating.

Original publication

DOI

10.1038/s41467-021-21283-4

Type

Journal article

Journal

Nature communications

Publication Date

02/2021

Volume

12

Addresses

Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia. k.kemper@uq.edu.au.

Keywords

Humans, Body Mass Index, Regression Analysis, Phylogeny, Inheritance Patterns, Quantitative Trait, Heritable, Linkage Disequilibrium, Phenotype, Polymorphism, Single Nucleotide, Genome, Human, Models, Genetic, Adult, Aged, Middle Aged, Educational Status, Biological Specimen Banks, United Kingdom