CHR = Chromosome BP = Basepair (GRCh37 build) SNP = SNP IDs are from 1000 Genomes Project (Phase I, Version 3) VAR = Variant allele REF = Reference allele ALL.FREQ.VAR = Frequency of variant allele in all GWAS1+2 patients ALL.RANDOM.BETA = Average change in Consortium lung phenotype for each copy of the variant allele in all GWAS1+2 patients, based on a random effects model ALL.RANDOM.PVAL = Meta-analysis P value in all GWAS1+2 patients, based on a random effects model (primary P value) ALL.FIXED.BETA = Average change in Consortium lung phenotype for each copy of the variant allele in all GWAS1+2 patients, based on a fixed effects model ALL.FIXED.PVAL = Meta-analysis P value in all GWAS1+2 patients, based on a fixed effects model FF.FREQ.VAR = Frequency of variant allele in p.Phe508del/p.Phe508del subset FF.RANDOM.BETA = Average change in Consortium lung phenotype for each copy of the variant allele in p.Phe508del/p.Phe508del subset, based on a random effects model FF.RANDOM.PVAL = Meta-analysis P value in p.Phe508del/p.Phe508del subset, based on a random effects model FF.FIXED.BETA = Average change in Consortium lung phenotype for each copy of the variant allele in p.Phe508del/p.Phe508del subset, based on a fixed effects model FF.FIXED.PVAL = Meta-analysis P value in p.Phe508del/p.Phe508del subset, based on a fixed effects model ***Variant allele is not necessarily the minor allele***