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GENOME-WIDE ASSOCIATION ANALYSES BASED ON WHOLE-GENOME SEQUENCING IN SARDINIA PROVIDE INSIGHTS INTO REGULATION OF HEMOGLOBIN LEVELS

机译:基于全基因组测序的撒丁岛全基因组关联分析为调节血红蛋白水平提供了思路

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摘要

We report GWAS results for the levels of A1, A2 and fetal hemoglobins, analyzed for the first time concurrently. Integrating high-density array genotyping and whole-genome sequencing in a large general population cohort from Sardinia, we detected 23 associations at 10 loci. Five are due to variants at previously undetected loci: MPHOSPH9, PLTP-PCIF1, FOG1, NFIX, and CCND3. Among those at known loci, 10 are new lead variants and 4 are novel independent signals. Half of all variants also showed pleiotropic associations with different hemoglobins, which further corroborated some of the detected associations and revealed features of coordinated hemoglobin species production.
机译:我们报告了首次同时分析的GWAS的A1,A2和胎儿血红蛋白水平。在一个来自撒丁岛的大型普通人群中整合了高密度阵列基因分型和全基因组测序,我们在10个位点检测到23个关联。五个是由于以前未检测到的基因座的变异引起的:MPHOSPH9,PLTP-PCIF1,FOG1,NFIX和CCND3。在已知基因座中,有10个是新的先导变异体,有4个是新的独立信号。所有变体中的一半还显示出与不同血红蛋白的多效性关联,这进一步证实了某些检测到的关联,并揭示了血红蛋白物种协调产生的特征。

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