rs12220128 - XRCC6P1 - RPL17P34

Magnitude 2.2 · 1 study on file

Reported associations

• Clinical trait-specific genetic analysis in Behçet's disease identifies novel loci associated with ocular and neurological involvement - Unknown journal (n.d.) · Unknown authors · PubMed 37271218

  ABSTRACT: Behçet's disease is a complex inflammatory vasculitis with a broad spectrum of clinical manifestations. The purpose of this study was to investigate the genetics underlying specific clinical features of Behçet's disease in a group of patients with > 20 years of follow up. A total of 436 patients with Behçet's disease from Turkey were studied. Genotyping was performed using the Infinium ImmunoArray-24 BeadChip. After imputation and quality control measures, logistic regressions adjusting for sex and the first five principal components were performed for each clinical trait using a case-case genetic analysis approach. A weighted genetic risk score was calculated for each clinical feature. Genetic association analyses of previously identified susceptibility loci in Behçet

Auto-generated from study metadata. AI-synthesised commentary is added when this entry is regenerated through content-service's LLM mode.