P-values are for test of difference in additive allelic and genotype distributions between diagnostic groups, adjusted for age and gender and relatedness. n = count; f = frequency. NC = could no
Loci were defined by the set of all SNPs in LD (r2 > 0.6, 1000 Genomes Phase 3 European samples) with an independently significant SNP (p 9] are indicated in bold text. (XLSX)