George Richenberg PhD thesis - Supplementary table 6.7: Summary statistics for sfFDR-identified novel genome-wide significant (FP<5x10-8), independent lead variants associated with CH risk in European ancestry individuals, compared with overall (inc) CH associations in African, East Asian, and South Asian ancestries

Summary statistics for novel, genome-wide significant (FP< 5×10⁻⁸), independent lead variants associated with CH risk identified using the sfFDR method in individuals of European ancestry (25,657 cases and 342,869 controls). These variants are compared with overall (inc) CH risk associations in individuals of African (375 cases; 8,168 controls), East Asian (101 cases; 2,043 controls), and South Asian (494 cases; 9,041 controls) ancestries.