Systematic assessment of COVID-19 host genetics using whole genome sequencing data.

PLoS Pathog · 2024 · PMC11706450 · PMID 39715278

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nominally significantno p-value reported

Some nominally significant results were observed.

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highly significantno p-value reported

While these results do not withstand statistical correction and warrant independent replication, they are complementing a recent study which identified a highly significant depletion of 3’UTR variants in the gene IL18RAP in amyotrophic lateral sclerosis (ALS) patients [ 49 ].

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