Identification of Novel Non-coding Genetic Variants of Serum Urate Using Whole Genome Sequencing in 7,339 Chinese
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The authors aimed to investigate the genetic architecture of low-frequency and rare variants associated with serum urate (SU) levels in East Asian populations, specifically focusing on their implications for gout and cardiometabolic diseases. Through whole-genome sequencing of 7,339 Han Chinese participants, they identified novel male-specific loci and rare variants that may influence SU regulation, enhancing understanding of the genetic factors contributing to SU levels and potential targets for precision therapies.
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