rs117625825 - EIF1AD

Magnitude 2.2 · 1 study on file

Reported associations

• A population-specific low-frequency variant of SLC22A12 (p.W258) explains nearby genome-wide association signals for serum uric acid concentrations among Koreans* - Unknown journal (n.d.) · Unknown authors · PubMed 32271837

  ABSTRACT: Prolonged hyperuricemia is a cause of gout and an independent risk factor for chronic health conditions including diabetes and chronic kidney diseases. Genome-wide association studies (GWASs) for serum uric acid (SUA) concentrations have repeatedly confirmed genetic loci including those encoding uric acid transporters such as ABCG2 and SLC9A2. However, many single nucleotide polymorphisms (SNPs) found in GWASs have been common variants with small effects and unknown functions. In addition, there is still much heritability to be explained. To identify the causative genetic variants for SUA concentrations in Korean subjects, we conducted a GWAS (1902 males) and validation study (2912 males and females) and found four genetic loci reaching genome-wide significance on chromosomes 4 (

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