i.
Read the research
Read summaries of published research in the marker library
TeleGenomics
Empowering Healthy Choices With Genomics
Explore the marker library or join the waitlist for consultations about a DNA report you already have
- Privacy information
- Genetics education
- Clear evidence limits
What we do
ii.
Prepare your questions
Use your report and family history to prepare questions for a healthcare professional
iii.
Consultation updates
Join the waitlist to hear when consultations are available
How we grade evidence
Each library entry includes a note about the available evidence.
You can see what a source supports, what remains uncertain, and what cannot be concluded from one finding.
- 01StrongClinical consensus
- 02ValidatedGuideline backed
- 03ModerateReplicated findings
- 04EmergingActive research
- 05ExploratoryEarly signal
Common Concerns With Direct-to-Consumer DNA Testing
Why Consult a Doctor?
Direct-to-consumer (DTC) DNA tests can offer valuable insights into your genetic makeup. However, interpreting these results can be complex and sometimes worrisome. Consulting with a doctor can help you understand your results and their potential implications for your health.
Remember, DTC tests are not diagnostic. Any major medical concerns identified should be assessed and diagnosed by a qualified doctor.
When to Consult a Doctor?
If your DNA test results indicate markers for conditions such as cancer, heart disease, or genetic disorders, please inform your family doctor or consult a healthcare professional. They can provide personalized advice, recommend further testing, and help you understand your options.
Use the marker library to look up genetic findings and prepare questions about your report
Bring the original report to a consultation so the result can be read with its source information
Important DNA Markers to Discuss With Your Doctor or Genetic Counselor
- BRCA1 and BRCA2: An educational entry on how researchers study inherited variants in family health history.
- MCM6: This marker is associated with lactase persistence or lactose intolerance, notably SNP rs4988235.
- FTO: Linked to obesity and type-2 diabetes, particularly the SNP rs9939609.
- APOE: Associated with Alzheimer's disease, including SNPs rs429358 and rs7412.
- TCF7L2: This marker is linked to type-2 diabetes, especially SNP rs7903146.
- OPRM1: Associated with opioid and alcohol dependence, notably SNP rs1799971.
- CDKN2A/B: An educational entry on how researchers examine inherited variation and heart health.
- CHRNA3: An educational entry on how inherited variation is studied alongside nicotine-use behaviour.
- CFTR: Associated with cystic fibrosis, notably mutations ΔF508 (rs113993960) and G551D (rs113993959).
- MTHFR: An educational entry about a gene involved in folate processing and the limits of single-variant interpretation.
- KCNJ11: Associated with type-2 diabetes, especially SNP rs5219 (E23K).
Explore DNA markers
A small selection of educational entries with source links, uncertainty notes, and questions to consider.
We know this genomic information can be heavy, so we have gathered some news articles that might brighten your day, feel free to visit Happy Good News and Genomes News for the best and brightest news articles we could find today.
Interested in personalized guidance?
Join the consultation waitlist or explore the genetics education library
Join the WaitlistSteps to get started
Get started
- Step 1
Browse the education library and note the topics you want to understand.
- Step 2
Join the waitlist for consultations about DNA reports you already have
- Step 3
Check consultation availability before sharing your report
Frequently asked questions
What is Telegenomics?
Telegenomics uses telehealth to deliver genomic services. It involves consultations with geneticists to interpret your genetic data and provide personalized health recommendations.
Are consultations available?
Consultations are not available to book yet. Join the waitlist for updates
Can I share a genetic report now?
New report sharing is paused. The education library remains available without an upload, and accepted formats will be published before intake opens.
How is genetic information handled?
Our privacy policy explains how genetic information is stored, used, and shared.
What if something in my report concerns me?
Take the original report to a qualified healthcare professional who can consider it alongside your personal and family history. Access and costs vary by location and by the professional you contact.
How are consultations conducted?
Check consultation availability before sharing your report
Understanding SNPs and the Human Genome
The Complexity of the Human Genome
People share most of their DNA, with many small differences from one person to another. Researchers study these differences to learn about inherited traits, but one difference alone does not provide a complete picture of a person's health.
What is an SNP?
A single nucleotide polymorphism, or SNP, is a variation at a single position in a DNA sequence among individuals. SNPs are the most common type of genetic variation and can act as biological markers, helping scientists locate genes associated with disease.
