Lowest cash-pay price in the industry

Sick with no answers?
It might be genetic.

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 qualify
No insurance required
Results in 4–6 weeks
Clinical-grade, physician-reviewed
5–7 yrs
Average time to rare disease diagnosis
~400M
People worldwide with a rare disease
~40%
Receive a diagnosis from genome sequencing
80%
Of rare diseases are genetic in origin
Accessible to every patient

Whole genome sequencing at the lowest cash-pay price

Most providers charge thousands of dollars for clinical whole genome sequencing. We don't think cost should stand between you and a diagnosis.

For every patient

Clinical Whole Genome Sequencing

The lowest cash-pay price in the industry.

No insurance required. No hidden fees. Accessible to any and every patient.

See if you're a candidate

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.


Sound familiar?

The diagnostic odyssey is real

If you've been searching for answers, you're not alone. Most people with an undiagnosed condition have experienced this:

Specialist after specialist

The average rare disease patient sees 7+ doctors before getting a diagnosis — if they ever get one.

Symptoms that don't add up

Multiple seemingly unrelated issues — neurological, developmental, metabolic — that no single diagnosis explains.

×

"Everything looks normal"

Standard blood work and imaging come back fine, but you know something isn't right.

Being dismissed

"It's anxiety." "It's stress." When standard tests can't explain it, some doctors stop looking.


Free screening

Could genetic testing help you?

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.

Who is the patient?

We'll tailor our assessment based on this.

What symptoms are you dealing with?

Describe in your own words — there are no wrong answers.

How long have symptoms been present?

Genetic conditions are typically present from birth, even if symptoms appear later.

How many doctors have you seen for this?

Include any specialist consulted about these symptoms.

Have you had genetic testing before?

Panel tests, exome sequencing, or chromosomal microarray — not consumer tests like 23andMe.

If this test could give you a definitive answer, what would that be worth to you?

Be honest — there's no wrong answer. This helps us understand how to make testing accessible.

You may be a strong candidate.

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.

Get started → What to expect first
?

You might benefit from testing.

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.

Schedule a free consultation → Learn more

This test may not be 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.

Explore other options →

You have a diagnosis — now what?

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.

Explore treatment options →

Transparency

What to actually expect

We believe in honesty. Here's the real picture:

~40% diagnostic rate

This is the real number from published studies. The most powerful single test available — but it doesn't find an answer for everyone.

For inherited conditions

This test identifies genetic variants you were born with. It's not for cancer screening, infections, or acquired conditions.

Best for the undiagnosed

Highest yield in patients with symptoms suggestive of a genetic condition who haven't found answers through standard workup.

A diagnosis ≠ a cure

Finding the cause is a critical first step. For some conditions there are treatments; for others, it opens doors to research and emerging therapies.

Not a replacement for your doctor

This screening is informational only. Genetic testing should always involve a qualified healthcare provider who can interpret results in context.


Common questions

FAQ

What is whole genome sequencing?
Whole genome sequencing reads your entire DNA — all 3 billion base pairs across ~20,000 genes. Unlike gene panels that check a handful of genes, it can find variants across your entire genome, including regions other tests miss.
How is this different from 23andMe?
Consumer tests look at ~0.02% of your genome for ancestry and wellness. Clinical whole genome sequencing analyzes 100% at high depth and is interpreted by medical geneticists for diagnostic purposes.
Why only ~40%? What about the other 60%?
The cause may be in a part of the genome we don't yet fully understand, may involve multiple genes, or may not be genetic. As science advances, some unsolved cases get re-analyzed and diagnosed later.
How much does it cost?
Clinical whole genome sequencing typically runs $1,500–$5,000 depending on the provider and insurance. Some programs offer financial assistance. We can help you understand your options.
Can insurance cover this?
Increasingly, yes — especially when ordered by a geneticist and you meet clinical criteria (which many undiagnosed patients do). Prior authorization helps. We navigate this with you.
What happens after a diagnosis?
A genetic diagnosis can change everything — connecting you with the right specialists, patient communities, clinical trials, and emerging therapies. For ultra-rare conditions, it can open the door to personalized treatments.

You've waited long enough.

Take 2 minutes to see if whole genome sequencing could find what everyone else has missed.

Take the free screening