Evaluation of reported pathogenic variants and their frequencies in a Japanese population based on a whole-genome reference panel of 2049 individuals. Issue 2 (February 2018)

• Record Type: Journal Article
• Authors: Yamaguchi-Kabata, Yumi; Yasuda, Jun; Tanabe, Osamu; Suzuki, Yoichi; Kawame, Hiroshi; Fuse, Nobuo; Nagasaki, Masao; Kawai, Yosuke; Kojima, Kaname; Katsuoka, Fumiki; Saito, Sakae; Danjoh, Inaho; Motoike, Ikuko; Yamashita, Riu; Koshiba, Seizo; Saigusa, Daisuke; Tamiya, Gen; Kure, Shigeo; Yaegashi, Nobuo; Kawaguchi, Yoshio; Nagami, Fuji; Kuriyama, Shinichi; Sugawara, Junichi; Minegishi, Naoko; Hozawa, Atsushi; Ogishima, Soichi; Kiyomoto, Hideyasu; Takai-Igarashi, Takako; Kinoshita, Kengo; Yamamoto, Masayuki
• Is Part Of: Journal of human genetics. Volume 63:Issue 2(2018)
• Page Start: 213
• Page End: 230
• Publication Date: 2018-02
• Subjects: Medical genetics -- Periodicals; Human genetics -- Periodicals; 616.042
• DOI: 10.1038/s10038-017-0347-1
• Languages: English
• ISSNs: 1434-5161

Abstract

Abstract Clarifying allele frequencies of disease-related genetic variants in a population is important in genomic medicine; however, such data is not yet available for the Japanese population. To estimate frequencies of actionable pathogenic variants in the Japanese population, we examined the reported pathological variants in genes recommended by the American College of Medical Genetics and Genomics (ACMG) in our reference panel of genomic variations, 2KJPN, which was created by whole-genome sequencing of 2049 individuals of the resident cohort of the Tohoku Medical Megabank Project. We searched for pathogenic variants in 2KJPN for 57 autosomal ACMG-recommended genes responsible for 26 diseases and then examined their frequencies. By referring to public databases of pathogenic variations, we identified 143 reported pathogenic variants in 2KJPN for the 57 ACMG recommended genes based on a classification system. At the individual level, 21% of the individuals were found to have at least one reported pathogenic allele. We then conducted a literature survey to review the variants and to check for evidence of pathogenicity. Our results suggest that a substantial number of people have reported pathogenic alleles for the ACMG genes, and reviewing variants is indispensable for constructing the information infrastructure of genomic medicine for the Japanese population.