RT Journal Article
SR Electronic
T1 Partitioning gene-level contributions to complex-trait heritability by allele frequency identifies disease-relevant genes
JF bioRxiv
FD Cold Spring Harbor Laboratory
SP 2021.08.17.456722
DO 10.1101/2021.08.17.456722
A1 Kathryn S. Burch
A1 Kangcheng Hou
A1 Yi Ding
A1 Yifei Wang
A1 Steven Gazal
A1 Huwenbo Shi
A1 Bogdan Pasaniuc
YR 2021
UL http://biorxiv.org/content/early/2021/08/18/2021.08.17.456722.abstract
AB Recent works have shown that SNP-heritability—which is dominated by low-effect common variants—may not be the most relevant quantity for localizing high-effect/critical disease genes. Here, we introduce methods to estimate the proportion of phenotypic variance explained by a given assignment of SNPs to a single gene (genelevel heritability). We partition gene-level heritability across minor allele frequency (MAF) classes to find genes whose gene-level heritability is explained exclusively by “low-frequency/rare” variants (0.5% ≤ MAF < 1%). Applying our method to ~17K protein-coding genes and 25 quantitative traits in the UK Biobank (N=290K), we find that, on average across traits, ~2.5% of nonzero-heritability genes have a rare-variant component, and only ~0.8% (370 gene-trait pairs) have heritability exclusively from rare variants. Of these 370 gene-trait pairs, 37% were not detected by existing gene-level association testing methods, likely because existing methods combine signal from all variants in a region irrespective of MAF class. Many of the additional genes we identify are implicated in phenotypically related Mendelian disorders or congenital developmental disorders, providing further evidence of their trait-relevance. Notably, the rare-variant component of gene-level heritability exhibits trends different from those of common-variant gene-level heritability. For example, while total gene-level heritability increases with gene length, the rare-variant component is significantly larger among shorter genes; the cumulative distributions of gene-level heritability also vary across traits and reveal differences in the relative contributions of rare/common variants to overall gene-level polygenicity. We conclude that the proportion of gene-level heritability attributable to low-frequency/rare variation can yield novel insights into complex-trait genetic architecture.Competing Interest StatementThe authors have declared no competing interest.