common variants cohort

Aliases

543 common SNPs (MAF ≥ 0.05), Common variants, Illumina markers, MAF ≥1% variants, SNP, SNPs, all common SNPs, common SNP, common SNPs, common SNPs of small effect, common alleles, common disease associated variant, common gene variant, common genetic variants, common genetic variation, common loci, common single nucleotide polymorphism, common single nucleotide polymorphisms, common variant, common variant association, common variants, common variants (MAF >5%), common variation, common variations, common, genome-wide SNPs, common-disease/common-variant, genome-wide SNPs, high-frequency variant, highly common variants, individual common variants, single nucleotide polymorphisms

Related entities (19)

Mentioned in (25)

Papers in which this entity is mentioned.

• Genome-wide association testing beyond SNPs. (2025)
• Genome-wide analyses identify 30 loci associated with obsessive-compulsive disorder. (2025)
• A statistical framework for multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2025)
• Transcription start sites experience a high influx of heritable variants fueled by early development. (2025)
• Improving polygenic risk prediction in admixed populations by explicitly modeling ancestral-differential effects via GAUDI. (2024)
• Osteosarcoma PDX-Derived Cell Line Models for Preclinical Drug Evaluation Demonstrate Metastasis Inhibition by Dinaciclib through a Genome-Targeted Approach. (2024)
• Recent advances in polygenic scores: translation, equitability, methods and FAIR tools. (2024)
• A harmonized public resource of deeply sequenced diverse human genomes. (2024)
• A statistical framework for powerful multi-trait rare variant analysis in large-scale whole-genome sequencing studies. (2023)
• Research Review: A guide to computing and implementing polygenic scores in developmental research. (2022)
• Variant interpretation using population databases: Lessons from gnomAD. (2022)
• Large-scale collaboration in ENIGMA-EEG: A perspective on the meta-analytic approach to link neurological and psychiatric liability genes to electrophysiological brain activity. (2021)
• Rapid genotype imputation from sequence with reference panels. (2021)
• The mutational constraint spectrum quantified from variation in 141,456 humans. (2020)
• The mutational constraint spectrum quantified from variation in 141,456 humans (2019)
• A SNP panel for identification of DNA and RNA specimens. (2018)
• The Impact of Peer Substance Use and Polygenic Risk on Trajectories of Heavy Episodic Drinking Across Adolescence and Emerging Adulthood. (2017)
• Universal Patterns of Selection in Cancer and Somatic Tissues. (2017)
• Assessing the Pathogenicity of Insertion and Deletion Variants with the Variant Effect Scoring Tool (VEST-Indel). (2016)
• RNA splicing is a primary link between genetic variation and disease. (2016)
• A global reference for human genetic variation. (2015)
• Candidate gene-environment interaction research: reflections and recommendations. (2015)
• Transcriptome sequencing of a large human family identifies the impact of rare noncoding variants. (2014)
• Common biological networks underlie genetic risk for alcoholism in African- and European-American populations. (2013)
• An integrated encyclopedia of DNA elements in the human genome. (2012)

Merged raw entities (38)

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