Technical artifact drives apparent deviation from Hardy-Weinberg equilibrium at CCR5-∆32 and other variants in gnomAD

Author:

Karczewski Konrad J.ORCID,Gauthier Laura D.,Daly Mark J.

Abstract

AbstractFollowing an earlier report suggesting increased mortality due to homozygosity at the CCR5-∆32 allele1, Wei and Nielsen recently suggested a deviation from Hardy-Weinberg Equilibrium (HWE) observed in public variant databases as additional supporting evidence for this hypothesis2. Here, we present a re-analysis of the primary data underlying this variant database and identify a pervasive genotyping artifact, especially present at long insertion and deletion polymorphisms. Specifically, very low levels of contamination can affect the variant calling likelihood models, leading to the misidentification of homozygous individuals as heterozygous, and thereby creating an apparent depletion of homozygous calls, which is especially prominent at large insertions and deletions. The deviation from HWE observed at CCR5-∆32 is a consequence of this specific genotyping error mode rather than a signature of selective pressure at this locus.

Publisher

Cold Spring Harbor Laboratory

Reference6 articles.

1. CCR5-∆32 is deleterious in the homozygous state in humans;Nat. Med,2019

2. Deviations from Hardy Weinberg Equilibrium at CCR5-Δ32 in Large Sequencing Data Sets

3. Karczewski, K. J. , Francioli, L. C. , Tiao, G. & Cummings, B. B. Variation across 141,456 human exomes and genomes reveals the spectrum of loss-of-function intolerance across human protein-coding genes. BioRxiv (2019).

4. Integrative genomics viewer

5. Detecting and Estimating Contamination of Human DNA Samples in Sequencing and Array-Based Genotype Data

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