The question of Queen Victoria's biological paternity has attracted periodic scholarly attention since biographer A.N. Wilson first formally proposed in 2003 that her father may have been Sir John Conroy rather than Edward, Duke of Kent. Previous treatments of this hypothesis have foundered on a single genetic objection: that Conroy showed no symptoms of haemophilia, and therefore could not have transmitted the condition to Victoria. This paper argues that objection rests on a fundamental misunderstanding of X-linked inheritance. We propose a novel and testable hypothesis: that a carrier female in Conroy's maternal line, originating in County Roscommon, Connacht, Ireland, is a scientifically plausible and hitherto uninvestigated source of the F9 mutation identified in Victoria's Romanov descendants. This hypothesis draws on peer-reviewed evidence that Ireland has the world's highest prevalence of Haemophilia B at 1 in 12,500 males — more than twice the global baseline — driven by confirmed founder mutations; that Connacht, the province from which the Conroy family originated, represents the most genetically ancient and isolated Celtic population in Europe; and that the household at Amorbach in the summer and autumn of 1818, the estimated period of Victoria's conception, contained John Conroy as a resident member alongside the Duke and Duchess of Kent. We call for a two-arm genetic study comparing identified Irish Haemophilia B founder mutations against the known royal F9 mutation, and testing living female descendants of the Conroy line for carrier status. No such study has previously been proposed or conducted.