This report is only based on your genetic information and not on any other information that you have shared. This testing includes variants with proven association with a condition and does not screen for all variants. There may be other associated markers/variants not screened here. The report is not diagnostic in nature and should not be considered as one. What we report here is your genetic predisposition towards any health condition. If you are found to be at high risk for certain health conditions, it does not indicate that you have, or will develop the health condition. On the other hand, if you are found to be at low risk for certain health conditions, it does not indicate that you do not have, or will not develop the health condition. Whether a person develops a health condition or not, it depends on various factors such as genetic predisposition, lifestyle choices, exposure to hazardous material, environment and many more. The report provided here should be able to help you to assess your health status at the genetic level and make the right choices for your health. The genotype determination in this test assumes all DNA samples are diploid. If, by nature, a collected sample has atypical genome content, it may affect the genotype determination, and any predicted risk based on the genotypes. This report is solely based on genetic makeup of the individuals and mutations detected at the time of sample collection. Please consult your doctor before considering the recommendations. The Service Provider will not be held liable for any direct, indirect, consequential, special, punitive, exemplary, or any other damages arising from the use of this service and/or report.