Rare protein-coding variants implicate genes involved in risk of suicide death.
Ontology highlight
ABSTRACT: Identification of genetic factors leading to increased risk of suicide death is critical to combat rising suicide rates, however, only a fraction of the genetic variation influencing risk has been accounted for. To address this limitation, we conducted the first comprehensive analysis of rare genetic variation in suicide death leveraging the largest suicide death biobank, the Utah Suicide Genetic Risk Study (USGRS). We conducted a single-variant association analysis of rare (minor allele frequency <1%) putatively functional single-nucleotide polymorphisms (SNPs) present on the Illumina PsychArray genotyping array in 2,672 USGRS suicide deaths of non-Finnish European (NFE) ancestry and 51,583 NFE controls from the Genome Aggregation Database. Secondary analyses used an independent control s
SUBMITTER: DiBlasi E
PROVIDER: S-EPMC9292859 | biostudies-literature | 2021 Dec
REPOSITORIES: biostudies-literature
ACCESS DATA