IFIH1 and Kallmann syndrome: We also detected several variants significantly associated with anosmia: the p.Ala946Thr in IFIH1 gene (presence of anosmia = 36.4% vs. absence = 17.6%), the p.Arg218Cys in MAVS gene (presence of anosmia = 22.2% vs. absence = 5.3%), the p.Met1?