MyGenomeBox(Collectively the "Company") provides DNA data storage and genomic data based services. We do not provide any analysis or interpretation defined as: recommending or endorsing any specific course of action, resources, tests, physician or other health care providers, drugs, biologics, medical devices or other products, procedures, opinions, or other information.

The intended use of our services is for research, informational, and educational use only. We do not provide medical advice. We do not recommend or endorse any specific course of action, resources, tests, physician or other health care providers, drugs, biologics, medical devices or other products, procedures, opinions, or other information that may be mentioned on our website.

Genomics is only part of the picture of an individual's state of being. In addition, understanding of genetic information is evolving very rapidly. Only a trained Physician or other health care providers can assess your current state of health or disease, taking into account many factors, therefore, reliance on any information provided is solely at your own risk. Consumers should not make any medical decision based solely on the results of the Company's DNA apps without the advice of a physician or a qualified healthcare professional.

The reports from the Company are based on standard analysis from a Whole genome, Exome, Targeted Sequencing or genotyping data that do not provide any medical advice, diagnosis or treatment. Analyses and reports provided by the Company are for informational purposes only and are subject to change. You should consult your physician if you have questions regarding any medical condition. The results and analysis presented in the report have not been clinically validated. Any report from MyGenomeBox has not been cleared or approved by the FDA or similar government institutions.

Whole genome sequencing covers minimum 95% of your entire genome with an accuracy greater than 99.9% with 30X of genomics sequencing depth. The sequencing process is a minimum of 24X depth of data to assure the quality of the data and result. Exome sequencing roughly covers only 2-4% of your genome, mostly areas that are well known from a genetics perspective, with an average of 100X sequencing depth.

The Company contains third party information and apps and does not recommend or endorse any specific tests, information or procedures. Any third party content data is subject to change and is non-specific in nature and should never be used as a substitute for medical advice. Linked websites and apps may contain texts, graphics, or information that you may find offensive. The Company does not guarantee such third party contents and citations to be medically accurate, precise and up to date. The Company, its affiliates, and its partners have no control over and accept no responsibility for such materials. Any information provided by this platform should never be used to make a medical diagnosis or decision.