Common Genetic Variants
Common Genetic Variants is a type of genetic variant characterized by a minor allele frequency of 5% or greater in a given population, distinguishing it from rare variants by its higher prevalence and typically smaller individual effect size on disease susceptibility within the context of complex traits such as dementia.
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Variants
Common Variants
Parents
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An integrated map of genetic variation from 1,092 human genomes
The Structure of Haplotype Blocks in the Human Genome
Stacey Gabriel, S. F. Schaffner, Huy Nguyen et al. · Science · 2002 · 5.9K citations
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QIMR Berghofer Medical Research Institute, Australia
74 publications · 13.2K citations
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Harvard University
Cambridge, United States
120 h-index
2.1K publications
421.1K citations
Massachusetts General Hospital
Boston, United States
96 h-index
1.3K publications
339.9K citations

Broad Institute
Cambridge, United States
96 h-index
1.8K publications
624.3K citations
National Institutes of Health
Bethesda, United States
93 h-index
1.5K publications
235.5K citations
University of Cambridge
Cambridge, United Kingdom
88 h-index
1.5K publications
220K citations
University of Oxford
Oxford, United Kingdom
87 h-index
995 publications
292.2K citations

Karolinska Institutet
Stockholm, Sweden
84 h-index
1.1K publications
181.6K citations
University College London
London, United Kingdom
84 h-index
1.3K publications
202.1K citations
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87 publications · 36.8K citations
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151 publications · 14.2K citations
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359 publications · 18.2K citations
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91 publications · 15.7K citations
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85 publications · 9.5K citations
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