Evidence-graded, variant by variant.
Every report shows the variant, your genotype, the effect size and the strength of evidence. No black boxes.
The evidence behind every report.
What we analyse
ACTN3, APOE, MCT1, PPARGC1A and hundreds more.
How we get your results
From your sample to graded, ranked insight.
Research & publications
The peer-reviewed basis of each report.
Our blogs
Articles, guides and the latest science.
Transparent by design.
- The exact variants behind each finding
- Your genotype and its effect size
- A clear strength-of-evidence grade
- Links to the peer-reviewed papers
The science, answered.
We only report variants with replicated, peer-reviewed evidence linking them to a measurable trait or health outcome. Each one is reviewed by our science team and graded for strength of evidence before it reaches your report.
It tells you how confident the research is. A higher grade means larger, repeated studies; a lower grade means the finding is promising but still emerging. You always see the grade alongside the result, so you can weigh it appropriately.
Yes. Your data is encrypted, never sold, and only used to generate your reports. You can request deletion at any time.
Every report links to the peer-reviewed papers it draws on, so you — or your clinician — can read the primary source directly.