Our reports do not diagnose or treat any health condition. they are not a substitute for medical advice. If you're diagnosed with a certain health condition, follow your doctor's advice. The scores/gauges use the latest scientific studies. But they are not perfect and will change as the models improve.
People without risk variants can also develop health conditions. Genetics is not the whole story. Your health is most often a combination of genetics, lifestyle, and environmental factors. Great news, as this means that you can often change your lifestyle to lower your risk.
Results might be more accurate for some ethnic groups than others. it depends on the studies used in each report. Not everyone with risk variants will develop a health condition.
Due to updated new information, your reports will be completed in the near future.
We are pleased to apply our experience and scale to provide professional, fast, and highly affordable Low-pass whole genome sequencing (LP-WGS) services pro le based on your individual genetic content. With the agreement with the best laboratories around the world (USA, Germany, Turkey, Emirate, India, and China), Build Goal Health Company provides the best quality tests at a reasonable price in a shorter time answering. Thanks for trusting us.
The results provided to you are based on the latest scientific research that has been published as scientific papers in a peer-reviewed journal. Therefore it is not a medical diagnostic report. To analyze your genetic code from the DNA of your Saliva sample, the state-of-the-art genetic testing lab procedure has been used. We deciphered your genetic code and estimated how your genes can influence many different aspects of your life. LP-WGS is commonly depend on sequencing a genome to an average depth of less than 1x coverage. LP-WGS, combined with genotype imputation, offers an alternative approach to genotyping arrays for trait mapping and calculation of polygenic scores. Now you can use your personalized recommendations to maximize your genetic potential toward optimizing your goal to improve your life. Difficulty in Identifying Rare Variants: LP-WGS may not be able to identify rare variants in the genome due to its limited coverage. Limited Clinical Utility: LP-WGS may not be suitable for clinical applications as it does not provide enough information about the genome to make accurate diagnoses or treatment decisions.
Hope you enjoy discovering yourself!