Phenome-wide association study in 25,639 pregnant Chinese women reveals loci associated with maternal comorbidities and child health

Phenome-wide association studies (PheWAS) have been less focused on maternal diseases and maternal-newborn comorbidities, especially in the Chinese population. To enhance our understanding of the genetic basis of these related diseases, we conducted a PheWAS on 25,639 pregnant women and 14,151 newborns in the Chinese Han population using ultra-low-coverage whole-genome sequence (ulcWGS). We identified 2,883 maternal trait-associated SNPs associated with 26 phenotypes, among which 99.5% were near established genome-wide association study (GWAS) loci. Further refinement delineated these SNPs to 442 unique trait-associated loci (TALs) predicated on linkage disequilibrium R2 > 0.8, revealing that 75.6% demonstrated pleiotropy and 50.9% were located in genes implicated in analogous phenotypes. Notably, we discovered 21 maternal SNPs associated with 35 neonatal phenotypes, including two SNPs associated with identical complications in both mothers and children. These findings underscore the importance of integrating ulcWGS data to enrich the discoveries derived from traditional PheWAS approaches. [Display omitted] •Large-scale genome-wide PheWAS in Chinese population of pregnant women and neonates•Integrating NIPT and EHR data to enhance the discovery by PheWAS•Revealing the genetic determinants of maternal-newborn comorbidities Guo et al. studied the association between 5,957,600 variants and 317 disease phenotypes in 25,639 Chinese pregnant women and 14,151 newborns using NIPT and EHR data. This study informed potential associations between maternal and neonatal diseases, offering insights into risk loci predisposing comorbidities of mothers and children.