rs113398003 - PTPRD

Magnitude 2.2 · 1 study on file

Reported associations

  • Evaluation of Shared Genetic Susceptibility to High and Low Myopia and Hyperopia. - JAMA ophthalmology (2022) · Tideman JWL, Pärssinen O, Haarman AEG, Khawaja AP, Wedenoja J, Williams KM, Biino G, Ding X, Kähönen M, Lehtimäki T, Raitakari OT, Cheng CY, Jonas JB, Young TL, Bailey-Wilson JE, Rahi J, Williams C, He M, Mackey DA, Guggenheim JA · PubMed 33830181

    Uncertainty currently exists about whether the same genetic variants are associated with susceptibility to low myopia (LM) and high myopia (HM) and to myopia and hyperopia. Addressing this question is fundamental to understanding the genetics of refractive error and has clinical relevance for genotype-based prediction of children at risk for HM and for identification of new therapeutic targets. To assess whether a common set of genetic variants are associated with susceptibility to HM, LM, and hyperopia. This genetic association study assessed unrelated UK Biobank participants 40 to 69 years of age of European and Asian ancestry. Participants 40 to 69 years of age living in the United Kingdom were recruited from January 1, 2006, to October 31, 2010. Of the total sample of 502 682 partici


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Lifestyle context

Concrete actions anchored to the cited research. We do not prescribe, we describe.

Discuss with your doctor

  • PTPRD-associated myopia risk and management Moderate

    rs113398003 increases genetic predisposition to high myopia; early detection supports management planning

    review screening frequency and prevention strategies with eye care provider

Screening

  • vision screening for myopia Moderate

    PTPRD variant rs113398003 associates with increased genetic risk for high myopia

    annual vision exams with refractive error assessment