Amrita ChattopadhyayTZU-PIN LU2020-11-172020-11-1720202218-676Xhttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85090257046&doi=10.21037%2ftcr-20-2395&partnerID=40&md5=aa39c027d70a72f04efb210f70405457https://scholars.lib.ntu.edu.tw/handle/123456789/520921English[SDGs]SDG3copy number variation; disease burden; disease severity; ethnic group; gene frequency; gene linkage disequilibrium; gene locus; gene mutation; genetic association; genetic background; genetic similarity; genetic variability; genome-wide association study; genotype; haplotype; haplotype map; heritability; heterozygote; human; human genome; morbidity; Note; single nucleotide polymorphism; Taiwanese; whole genome sequencingnote10.21037/tcr-20-23952-s2.0-85090257046