SNPMiner Trials (Home Page)
Report for SNP rs2089760
Developed by Shray Alag, 2020.
SNP Clinical Trial Gene
There is one clinical trial.
Clinical Trials
1 TGFB1 and LAMA1 Gene Polymorphisms in Turkish Children With High Myopia
The investigators aimed to investigate TGFB1 and LAMA1 gene polymorphisms in children with high myopia in order to determine the genetic basis of large myopic shifts causing severe visual impairment and complications. Seventy-four children with high myopia (≥6 diopters [D]; study group) and 77 emmetropic children (±0.5D; control group) were included. Genetic and polymorphism analyses were performed in the Medical Genetics Laboratory using DNA purified from the patients' blood samples.
NCT03451877 High Myopia Gene Mutations Genetic: TGFB1 AND LAMA1 GENE POLYMORPHISMS MeSH:Myopia
HPO:Myopia
evaluated polymorphisms in the LAMA1 (rs2089760) and TGFB1 (rs4803455) genes in children younger than 13 years of age with ≥6 D myopia.
Primary Outcomes
Description: evaluated polymorphisms in the LAMA1 (rs2089760) and TGFB1 (rs4803455) genes in children younger than 13 years of age with ≥6 D myopia
Measure: Genetic basis of high myopia Time: 4 years