[3P-0656] Phenome scan of ZFHX3 gene variation: association with atrial fibrillation, cerebral infarction, and lung thromboembolism

〇Khin Thet Thet Zaw¹、Noriko Sato¹、Shinobu Ikeda¹、Kaung Si Thu¹、Makiko Naka-Mieno²、新井 冨生^3,4、Seijiro Mori⁵、Tetsushi Furakawa⁶、Tetsuo Sasano⁷、Motoji Sawabe⁸、田中 雅嗣⁹、Masaaki Muramatsu¹ (1.Department of Molecular Epidemiology, Medical Research Institute, Tokyo Medical and Dental University, Japan、2.Department of Medical Informatics, Center of Information, Jichii Medical University, Japan、3.Department of Pathology, Tokyo Metropolitan Geriatric Hospital, Japan、4.Research Team for Geriatric Pathology, Tokyo Metropolitan Institute of Gerontology, Japan、5.Center for Promotion of Clinical Investigation, Tokyo Metropolitan Geriatric Hospital, Japan、6.Department of Bioinformational Pharmacology, Medical Research Institute, Tokyo Medical and Dental University, Japan、7.Department of Biofunctional Informatics, Tokyo Medical and Dental University, Japan、8.Department of Moleculo-genetic Sciences, Division of Biomedical Laboratory Sciences, Molecular Pathophysiology, Graduate School of Health Care Sciences, Tokyo Medical and Dental University, Japan、9.Departmentof Genomics for Longevity and Health, Tokyo Metropolitan Institute of Gerontology, Japan)

ATBF1, atrial fibrillation, cerebral infarction, lung thromboembolism, single nucleotide polymorphism