(一)筛选变异MODY基因的全基因组测序。所有的变异或只显示中度或高度的影响。小说变异变异没有dbSNP id或者报告文学。在c (B)当地祖先单。1108G>T variant region for all 87 admixed and c.1108G>T heterozygous individuals. Each individual is represented with two lines, one for the c.1108G>T haplotype and one for the WT haplotype. The vertical line represents the position of the c.1108G>T variant. (C) Frequency of T2D separated by genotype and effect size (OR) with 95% CI below. (D) Mean value of HbA1c separated by genotype and effect size with 95% CI below. (E) Serum insulin measurements at fasting (0 min), 30-min, and 2-h after glucose ingestion of the follow-up participants. (F) Plasma glucose measurements at fasting (0 min), 30-min, and 2-h after glucose ingestion of the follow-up participants. In E and F errors are mean ± SEM. Credit:《柳叶刀》区域卫生——欧洲(2022)。DOI: 10.1016 / j.lanepe.2022.100529