Whole genome sequencing
Reads nearly all of your DNA. Powerful - but most findings are uncertain without expert review.
TypeGenetic
HowBlood or saliva sample.
How oftenOnce.
BeforeCounseling recommended.
WhoCurious users or specific clinical situations.
Your whole genetic code - and a lot to interpret
Whole genome sequencing reads nearly all of your DNA. It can reveal rare conditions, but also many changes of unknown meaning - so expert interpretation matters as much as the test.
Clear findings
“Is there a known risk?”
A small number of people learn about a serious, actionable risk.
Actionable
Uncertain findings
“What does this change mean?”
Many variants have unknown meaning and may be reclassified later.
Unclear
Re-analysis
“Can I use it later?”
Your data can be reviewed again as science improves.
Long-term value
Is it right for you?
Worth considering if…
- You want the most complete genetic picture and have access to expert interpretation.
- You have an unexplained condition that may be genetic.
- You want data that can be re-analysed as science advances.
A better option if…
- You have a specific question - a targeted clinical test is usually clearer.
How it’s measured
Clinical WGS
Interpreted by clinical geneticists.
Consumer WGS
Raw data with limited interpretation.
The full picture
What is it?
Sequencing of almost your entire genome.
What type of test is it?
A genetic test.
What does it measure?
Your DNA sequence.
Why might someone consider it?
Comprehensive genetic insight.
Who is it most relevant for?
Curious users or specific clinical cases.
How is it performed?
A blood or saliva sample.
How often might it be considered?
Once.
What can the result help you understand?
Known high-risk variants and much uncertain information.
What are its limitations?
Many variants of uncertain significance; privacy; cost.
What should it be viewed with?
Family history, clinical tests and counseling.
Where to get it
Through your provider
Often with a genetic counselor - and more likely covered when family history supports it.
Genetic counseling services
Help you decide what to test and what results mean.
Direct-to-consumer tests
Available, but results should be confirmed clinically before acting on them.
Names are examples only, not endorsements. Your provider can often order the same test - and help interpret it.
Connected to
Questions to ask your provider
- What would I do with the results?
Ziva Health
One test is a snapshot. Ziva shows the whole story.
Ziva brings your lab results, wearables and daily readings together - and Isabella tells you what’s changing and what to ask your provider next.
Refer Ziva to my provider / care team
Is your provider not on Ziva yet? Send them a link in under a minute - once they join, they’ll see your Whole genome sequencing result alongside your other trends and get alerts directly.
Refer my providerAlready seeing your provider?
Bring your Ziva 30-day report to your next appointment - your Whole genome sequencing result and daily trends in one view, so the conversation starts with the full picture.
Get my 30-day reportNo provider? Find a clinical partner
Being listed doesn’t mean everyone needs this test. Educational only — not medical advice. Results should be interpreted with a qualified clinician. ← Back to Know What to Test