myHealthScore 31 de Maggio de 2022 by Lascia un commento Descrizione Descrizione myHealthScore è il test di screening genetico che fornisce informazioni sul rischio di malattie multifattoriali comuni. Il test determina il rischio poligenico precedentemente non rilevato, consentendo di individuare un numero maggiore di persone a rischio. 260€ PURCHASE myHealthScore What is polygenic risk? The most common diseases tend to have multifactorial causes. In other words, they are produced due to genetic effects along with other factors, such as lifestyle habits and the environment. In these cases, the genetic risk is not usually associated with a single variant but with thousands or millions of common variants throughout the genome. This is known as a polygenic risk. Which diseases does myHealthScore study? Cardiovascular disease* >2 million variants Type 2 diabetes > 600.000 variants Breast cancer > 550.000 variants Prostate cancer > 650.000 variants You can request a myHealthScore for cardiovascular, type 2 diabetes or cancer risk, either separately or all together with more advantageous conditions. *For a more complete analysis of cardiovascular disease, the test includes the polygenic risk of: coronary artery disease, atrial fibrillation, lipid profile (triglyce – rides and cholesterol LDL and HDL) and high blood pressure. Purchase myHealthScore 260€ Include Cardiovascular disease analysis Hereditary breast cancer and prospate cancer analysis data Type 2 Diabetes analysis PURCHASE myHealthScoremyHealthScore include Whole genome sequencing technology and analysis with CE-IVD software.Analysis of thousands to millions of variants related to the conditions analyzed.Possibility of extending the assay to other conditions as the science advances.Access to Veritas calculator to assess the absolute risk based on genetic and clinical factors. How do I start? 1. Buy and recieve your test Veritas provides a kit with which to obtain the patient’s saliva. 1. Provides your sample The patient provides the sample. 3. Analysis of your sample and inssuece results The sample is processed, the sequencing is carried out using NGS technology and the analysis is made using EC branded software. 4. Delivery of results Results are provided with relevant content for the medical care of the patient.
