Millions spend years bouncing between doctors with no diagnosis. Whole genome sequencing finds a genetic diagnosis in ~40% of undiagnosed patients — and we make it accessible to every patient at the lowest cash-pay price in the industry.
See if you qualifyMost providers charge thousands of dollars for clinical whole genome sequencing. We don't think cost should stand between you and a diagnosis.
The lowest cash-pay price in the industry.
No insurance required. No hidden fees. Accessible to any and every patient.
No insurance needed. We offer the lowest cash-pay price in the industry — no surprise bills, no prior authorization hoops, no waiting. If you do have insurance, we can help with coverage too.
If you've been searching for answers, you're not alone. Most people with an undiagnosed condition have experienced this:
The average rare disease patient sees 7+ doctors before getting a diagnosis — if they ever get one.
Multiple seemingly unrelated issues — neurological, developmental, metabolic — that no single diagnosis explains.
Standard blood work and imaging come back fine, but you know something isn't right.
"It's anxiety." "It's stress." When standard tests can't explain it, some doctors stop looking.
Answer a few quick questions. This isn't a medical diagnosis — it's a simple check to see if whole genome sequencing might be your right next step.
We'll tailor our assessment based on this.
Describe in your own words — there are no wrong answers.
Genetic conditions are typically present from birth, even if symptoms appear later.
Include any specialist consulted about these symptoms.
Panel tests, exome sequencing, or chromosomal microarray — not consumer tests like 23andMe.
Be honest — there's no wrong answer. This helps us understand how to make testing accessible.
Whole genome sequencing could help find your answer.
Based on your answers, your situation aligns with cases where whole genome sequencing has the highest diagnostic yield — approximately 40% of patients in a similar position receive a definitive genetic diagnosis.
A single test analyzing all ~20,000 genes at once could potentially end years of searching.
There's more to consider first.
Your situation has some indicators that genetic testing could help, but the diagnostic yield may vary. Overall, whole genome sequencing finds an answer in ~40% of cases — a brief consultation could help determine if this is right for you.
But other options may be worth exploring.
Whole genome sequencing is designed for inherited genetic conditions — it isn't a general diagnostic tool. Based on your answers, other types of evaluation may be more appropriate right now.
A diagnosis is the starting point, not the end.
If you have a genetic diagnosis but no available treatment, you may be a candidate for emerging personalized therapies — including custom antisense oligonucleotides, gene therapy, or other precision approaches for rare diseases.
We believe in honesty. Here's the real picture:
This is the real number from published studies. The most powerful single test available — but it doesn't find an answer for everyone.
This test identifies genetic variants you were born with. It's not for cancer screening, infections, or acquired conditions.
Highest yield in patients with symptoms suggestive of a genetic condition who haven't found answers through standard workup.
Finding the cause is a critical first step. For some conditions there are treatments; for others, it opens doors to research and emerging therapies.
This screening is informational only. Genetic testing should always involve a qualified healthcare provider who can interpret results in context.
Take 2 minutes to see if whole genome sequencing could find what everyone else has missed.
Take the free screening