Find the Variants That Matter

From raw DNA to a clear, doctor-ready plan for your health

We review every variant in your genome, highlight the ones that matter most, and give you the evidence you need to take the next step toward answers.

Variant Interpretation

We turn your raw genetic data into a complete, easy-to-use file and highlight the most important variants for review.

One-on-one help, tailored to your health history and goals, with reports designed for your doctor to actually read.

Easy-to-read summaries, relevant research links, and practical next steps to take to your medical team.

Personalized Support
Clear Reports

Deep Variant Research

We go deeper than basic summaries, digging into the science behind your genetic findings. That includes peer-reviewed studies, clinical variant databases, rare disease references, and more, all curated to fit your specific genetic profile. Whether you're navigating a VUS, a rare condition, or an unclear diagnosis, we provide well-researched information and meaningful next steps tailored to you.

A collection of items related to a test kit, including a white and blue box labeled 'testalize.me', a sealed return envelope, a small vial, an information booklet, a code card, a pipette, and a clear plastic bag with a blue strip.
A collection of items related to a test kit, including a white and blue box labeled 'testalize.me', a sealed return envelope, a small vial, an information booklet, a code card, a pipette, and a clear plastic bag with a blue strip.
We go beyond surface-level reports to dig into the science behind your DNA.

Genetic Insights Delivered

We turn your raw genetic data into clear, easy-to-read reports that highlight your most important variants, explain what they mean, and connect you to the latest research. Every summary is designed to support your medical appointments, help with family discussions, and guide your own health advocacy.

One-on-One Variant Guidance

We work with you personally to identify your next steps. Whether you’re reaching out to labs, joining rare disease registries, or preparing for a specialist appointment, we tailor our support to match your goals not just your genes.

gray concrete building during daytime
gray concrete building during daytime
In-Depth Research and Resources

We dig deep into trusted genetic databases and peer-reviewed studies to uncover what’s known about your variants. You’ll get relevant publications, rare disease references, and curated tools chosen specifically for your results and goals.

A detailed digital depiction of a DNA helix structure, with strands intertwined and illuminated in contrasting hues. The image is set against a dark background, highlighting the bright blues and pinks that represent the complex molecular formation. The strands are intricately detailed, resembling a flowing pattern of dots and lines that suggest motion and energy.
A detailed digital depiction of a DNA helix structure, with strands intertwined and illuminated in contrasting hues. The image is set against a dark background, highlighting the bright blues and pinks that represent the complex molecular formation. The strands are intricately detailed, resembling a flowing pattern of dots and lines that suggest motion and energy.
red blue and black abstract painting

Get Your Genome Review Started

Tell us a little about your genetic data and goals so we can help you take the next step.