George Richenberg PhD thesis - Supplementary table 6.2: Summary statistics for the monoallelic genome-wide significant (P<5x10-8), independent lead variants associated with overall (inc) CH risk in the UKB compared with the 15 blood cell traits in BCX2

This dataset compared summary statistics for 21 monoallelic genome-wide significant (P<5×10⁻⁸), independent lead variants associated with overall (inc) CH risk in 368,526 individuals (25,657 cases; 342,869 controls) of European ancrestry in the UK Biobank (PMID: 36450978) with 15 blood cell traits in 562,132 individuals of European ancestry from the Blood Cell Consortium (Phase 2) (PMID: 32888493).