About Us

About Us

Uturn9 Genetic

Uturn9 genetics is a mission to help people access, understand and benefit from the human genome. Based in the UAE, Uturn9 is a sister concern of SWAFE Wellness. A company that aims at making people disease free and manage to live a life tablet free. Uturn9 is driven by the idea of Non-invasive diagnostics that takes you to the core of human existence, your DNA. With state of the art and highly advanced Technology labs in Germany, Uturn9 brings you the most accurate information and diagnostics facilitated by Expert Genetics scientists based in Germany.
  • Uturn9 has more than 12,000,000 customers.
  • More than 80 percent of our customers have opted-in to participate in our research.
  • To date, the company has collected three billion phenotypic data points (individual survey responses).
  • On average, one individual contributes to 200 different research studies.
  • To date, Uturn9 has published more than 150 peer-reviewed studies in scientific journals.

Our Vision

Our excellent team is ready to be part of your team to work into the different areas of diagnoses. Scientists helping scientists.

We Are The Trusted Experts

We are a mission-driven company with big dreams of using data to revolutionize health, wellness and research. We want to improve healthcare. We want to prevent disease. We want to give individuals control over their health data. We want to dramatically accelerate the pace of research. We want to develop better drugs smarter and faster. There is no comfort zone. We do not shy away from controversy, and we never give up. We are pioneering a new world, centered on the consumer, where success depends on bold ideas and unprecedented scale. Big is key, and thinking big drives us.

This company is built on science. We make evidence-based decisions. In a world where health is poorly understood, we use data to better understand wellness and disease. We bring science to our customers and help them use it in meaningful ways. We are committed to scientific standards and being a trusted source of genetic information. At the same time, we push the boundaries of what’s possible to enable groundbreaking research and innovative products. And we empower those outside the company to leverage the platform we’ve built.

OVERVIEW

About DNA

Genetic Testing/DNA Testing

Genetic testing, also known as DNA testing, is used to identify changes in DNA sequence or chromosome structure. Genetic testing can also include measuring the results of genetic changes, such as RNA analysis as an output of gene expression, or through biochemical analysis to measure specific protein output.In a medical setting, genetic testing can be used to diagnose or rule out suspected genetic disorders, predict risks for specific conditions, or gain information that can be used to customize medical treatments based on an individual's genetic makeup. Genetic testing can also be used to determine biological relatives, such as a child's parentage (genetic mother and father) through DNA paternity testing, or be used to broadly predict an individual's ancestry. Genetic testing of plants and animals can be used for similar reasons as in humans (e.g. to assess relatedness/ancestry or predict/diagnose genetic disorders),to gain information used for selective breeding,or for efforts to boost genetic diversity in endangered populations.

The variety of genetic tests has expanded throughout the years. Early forms of genetic testing which began in the 1950s involved counting the number of chromosomes per cell.

Genetic testing is a type of medical test that identifies changes in genes, chromosomes, or proteins. The results of a genetic test can confirm or rule out a suspected genetic condition or help determine a person’s chance of developing or passing on a genetic disorder. More than 77,000 genetic tests are currently in use, and others are being developed.

Genetic testing involves looking for changes in:

Genes : Gene tests study DNA sequences to identify variations (mutations) in genes that can cause or increase the risk of a genetic disorder. Gene tests can be narrow or large in scope, analyzing an individual DNA building block (nucleotide), one or more genes, or all of a person’s DNA (which is known as their genome).

Chromosomes : Chromosomal genetic tests analyze whole chromosomes or long lengths of DNA to see if there are large genetic changes, such as an extra copy of a chromosome, that cause a genetic condition.

Proteins : Biochemical genetic tests study the amount or activity level of proteins or enzymes; abnormalities in either can indicate changes to the DNA that result in a genetic disorder.

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