The kit will be sent directly to your doorstep. Register the kit online and swab the inner side of your cheek. Send your swab back for free.
Our ISO accredited labs will extract your DNA from the saliva sample and analyse it to identify your unique genetic profile.
Your genetic reports will undergo a thorough cardiologist and personal trainer assessments. The assessment will take into account your health, lifestyle and genetic profiles.
You will receive a tailored health, diet, exercise and lifestyle action plan. The reports will come with personalised medical assessment and 8 weeks tailored training and diet programs. All based on your environment and Genetic profile.
With your reports, you will have full access to our online support platform for booking follow up appointments with our partner specialists.
Orders can be placed on our website and we'll send the kit to your doorstep by post. You can also purchase it at one of our partner specialists’ facilities.
Yes, you can purchase as many kits as you wish. However, you can only register one kit per user.
Once you have received your saliva collection kit, you will need to register its unique barcode on our website, then create an account with a valid email address. To register your kit, please visit: www.rightangled.co/start
If you need specialised advice, you can book an appointment from your online portal with any of our partner specialists (Cardiologists, General Practitioners and Personal Trainers), you can book the appointment to take place over the phone or in-person, at the partner's facility.
For all general enquiries, you can chat with our support team directly using the chat bot on the bottom right corner of the webpage.
To ensure the efficacy of our service, we have partnered with ISO accredited labs that adhere to high standards of quality assurance and quality controls. Our gene panel list is assayed through a genotyping technology that utilises competitive allele-specific microarray technology, which enables highly accurate bi-allelic scoring of SNPs (99.8% accurate) and indels (insertions and deletions) at specific loci across a wide range of genomic DNA samples, thereby limiting the risk of false-positive and false-negative results.
Once the analysis is conducted, the reports are then reviewed by our specialist partners, along with your provided health profile, in order to deliver an accurate assessment for each individual result and to deliver personalised action plans on what you can do next.