Atrial fibrillation: the role of common and rare genetic variants

Medicin og biovidenskab

• Atrial Fibrillation 100%
• Genome-Wide Association Study 29%
• Single Nucleotide Polymorphism 23%
• Exome 16%
• Gain of Function Mutation 9%
• Loss of Function Mutation 7%
• Mutation 7%
• Cardiac Arrhythmias 5%
• Genes 5%
• Population 2%