Skip to main content
Fig. 1 | Orphanet Journal of Rare Diseases

Fig. 1

From: Systematic estimation of cystic fibrosis prevalence in Chinese and genetic spectrum comparison to Caucasians

Fig. 1

Overall Study design. This study consisted of four parts, and within each part, the systematically comparisons among our two cohorts (representing Chinese population) with public reported cohorts from gnomAD-NFE, 1000genome-NFE (representing Caucasian population) and gnomAD-EAS, 1000genome-EAS (control for east Asian population) were performed: (1) CFTR variant pathogenicity curation. (2) CF retrospectively identification. (3) CF affected frequency estimation. (4) CFTR gene haplotype estimation

Back to article page