![]() Panels and genes analyzed in my test from Invitae. Genotyping results do not eliminate the necessity to account for non-genetic factors that can influence dose. The FDA has recommended pharmacogenetic testing (PGx) only for specific drugs and does not yet mandate it for routine use in guiding therapeutic decisions for all drugs. Licensed medical practitioners are trained and qualified to make therapeutic decisions based on patient information and medical history, including the pharmacogenetic report. This report is to be interpreted only by a qualified and licensed medical practitioner Ancestry DNA tests do not cover all pharmacogenetic markers and are not considered to be clinically suitable. Here is part of the disclaimer from the Precision Medical Report: As I try to eat more healthy and keep fit I will refer to them to help design my plan.Įach Report contained a disclaimer. The reports were easy to read and provided some interesting items. The good news from the Health Reports were that I was not likely to gain weight on a high carb diet. The information provided must be interpreted only by a qualified physician.” from XCode Life. MTHFR (methylenetetrahydrofolate reductase) “ An MTHFR status report is one of the many indicators for identifying the risk of developing cardiovascular disease, or the risk for neural tube defects and sensitivity to methotrexate. ![]() It did give me a Pharmacological Report that assessed different drugs and their efficacy should I need to use them to treat Breast Cancer. The Breast Cancer Report just confirmed the other two reports that I received from 23 & Me and Invitae. Most of the information in this report had was that I wasn’t a carrier or the disease is so rare that it was not an issue for me. (Defination Mayo Clinic) It closed on both of us as babies. One of the carrier genes it reported was as follows: CONGENITAL HEART DISEASE Gene markers analyzed: 4 Gene markers present in your genome data: 1 Potential pathogenic variants found in your genome data: chr8:g.11612698C>A Genes analyzed: GATA4īoth my half sister and I on my maternal side had Ventricular Septal Defect – A ventricular septal defect ( VSD ), a hole in the heart, is a common heart defect that’s present at birth (congenital). ![]() This means you carry one variant for the condition. They provided 10 reports: Allergy Response, Breast Cancer, Carrier Status, Prime Fitness, Supreme Health, Methylation Report, Good Nutrition, Unique Personality, Precision Medicine and Radiant Skin.įor example the Carrier Status Report – can tell you about a variant that could affect you and could also affect the health of your future family.
0 Comments
Leave a Reply. |