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We built a reference panel with 342 million autosomal variants using 78,195 individuals from the Genomics England (GEL) dataset, achieving a phasing switch error rate of 0.18% for European samples and imputation quality of r2 = 0.75 for variants with minor allele frequencies as low as 2 × 10-4 in white British samples. The GEL-imputed UK Biobank genome-wide association analysis identified 70% of associations found by direct exome sequencing (P -11), while extending testing of rare variants to the entire genome. Coding variants dominated the rare-variant genome-wide association results, implying less disruptive effects of rare non-coding variants.

Original publication

DOI

10.1038/s41588-024-01868-7

Type

Journal article

Journal

Nature genetics

Publication Date

08/2024

Addresses

Department of Statistics, University of Oxford, Oxford, UK. sinan.shi@stats.ox.ac.uk.