[3P-925] Development of a reference database and toolkit for rare undiagnosed disease-specific epivariant analysis

^○Saki Aoto¹, Keiko Matsubara^3,2, Kazuki Yamazawa⁴, Kenichiro Hata^5,6, Masayo Kagami³, Kazuhiko Nayabayashi⁶ (1.Med.Gen.Ctr., NCCHD, 2.Dept. of Divers. Res., NCCHD, 3.Dept. of Mol. Endo., NCCHD, 4.Med. Genet. Ctr., NHO Tokyo Med. Ctr., 5.Dept. of Mol. and Cell. Biol., Grad. Sch. of Med., Gunma Univ., 6.Dept. of Mat. Fetal. biol., NCCHD)