Parkinson-Alzheimer-Dementia Genetic Test

Know your inherited neurodegeneration risk before symptoms appear

A comprehensive DNA test that screens 35 genes linked to Alzheimer's, Parkinson's, frontotemporal dementia, and inherited movement disorders.

$529$800Save $271

HSA / FSA eligible

Free shippingSpecimen:Buccal swabCollection:SelfCLIA-certified lab:FulgentResults:2-3 weeks

Simple Process

How it works

From order to insights in three easy steps — no doctor’s visit required.

Get Your Collection Kit

Your kit will arrive in about of a week of purchase. It includes everything you need to collect your DNA.

Collect Your Sample

You'll swab the inside of your mouth with the provided buccal swab. That's it. Send it back using the prepaid shipping label.

Receive Your Results

Results will be ready within 2-3 weeks after your sample arrives at the lab. You'll receive a detailed report with your results.

Is This Right for You?

This test is designed for people who

If any of these apply, this test can give you clarity and peace of mind.

Have a family history of Alzheimer's, Parkinson's, or other neurodegenerative diseases

Want to understand whether they carry inherited gene variants that increase risk for dementia or movement disorders

Are noticing early cognitive or motor changes and want to explore a genetic basis

Want proactive screening to guide lifestyle, monitoring, or clinical trial eligibility

Have been referred by a neurologist or genetic counselor for hereditary neurodegeneration screening

Are planning a family and want to know about inherited neurological conditions they could pass on

35 Genes · 6 Categories

What your report covers

Each category is reviewed by a board-certified geneticist and mapped to clinical guidelines.

Alzheimer's disease

Genes linked to inherited Alzheimer's disease. PSEN1 and PSEN2 cause rare early-onset forms, while APOE affects risk for the more common late-onset form.

Parkinson's disease

Genes tied to typical-onset Parkinson's disease. LRRK2 and GBA are the most common genetic risk factors and are actively being targeted by new therapies.

Young-onset Parkinson's & parkinsonism

Genes behind Parkinson's that starts before age 50. These tend to be recessive (inherited from both parents) and often progress more slowly.

Frontotemporal dementia & ALS overlap

Genes behind frontotemporal dementia (FTD), which affects personality and language. C9orf72 can cause both FTD and ALS in the same family.

Rare movement & dystonia disorders

Genes causing inherited dystonia and movement disorders. Some, like GCH1, respond very well to medication when diagnosed.

Rare inherited dementias

Genes behind rare forms of inherited dementia, including prion disease, CADASIL (small vessel strokes), and white matter disorders.

Trusted by Thousands

What customers say

Real results from real people taking control of their brain health.

★★★★★

“Turned my family history into a real action plan”

Both my parents developed Alzheimer’s and I was tired of just worrying. This test showed I carry an APOE ε4 allele, so I overhauled my exercise, sleep, and diet with my doctor. For the first time I feel like I’m actually doing something about it.

Linda M.58

★★★★★

“Knowing my LRRK2 status gave me a head start”

My uncle had Parkinson’s and I didn’t want to wait for symptoms to find out if I was at risk. The test identified a LRRK2 variant, so now I’m prioritizing high-intensity exercise, better sleep, and regular check-ins with my neurologist. I went from anxious to prepared.

Robert C.52

★★★★★

“Now my whole family has a prevention roadmap”

After my mother’s frontotemporal dementia diagnosis, I wanted answers — not just for me, but for my siblings. The test found a C9orf72 expansion. Now all three of us are working with our doctors on early monitoring and lifestyle changes we wouldn’t have known to make.

Angela D.41

Take the first step for your brain health

Know your genetic risks. Share with your doctor. Plan ahead with confidence.

Parkinson-Alzheimer-Dementia Genetic Test

Know your inherited neurodegeneration risk before symptoms appear

A comprehensive DNA test that screens 35 genes linked to Alzheimer's, Parkinson's, frontotemporal dementia, and inherited movement disorders.

$529$800Save $271

HSA / FSA eligible

Free shippingSpecimen:Buccal swabCollection:SelfCLIA-certified lab:FulgentResults:2-3 weeks

Simple Process

How it works

From order to insights in three easy steps — no doctor’s visit required.

Get Your Collection Kit

Your kit will arrive in about of a week of purchase. It includes everything you need to collect your DNA.

Collect Your Sample

You'll swab the inside of your mouth with the provided buccal swab. That's it. Send it back using the prepaid shipping label.

Receive Your Results

Results will be ready within 2-3 weeks after your sample arrives at the lab. You'll receive a detailed report with your results.

Is This Right for You?

This test is designed for people who

If any of these apply, this test can give you clarity and peace of mind.

Have a family history of Alzheimer's, Parkinson's, or other neurodegenerative diseases

Want to understand whether they carry inherited gene variants that increase risk for dementia or movement disorders

Are noticing early cognitive or motor changes and want to explore a genetic basis

Want proactive screening to guide lifestyle, monitoring, or clinical trial eligibility

Have been referred by a neurologist or genetic counselor for hereditary neurodegeneration screening

Are planning a family and want to know about inherited neurological conditions they could pass on

35 Genes · 6 Categories

What your report covers

Each category is reviewed by a board-certified geneticist and mapped to clinical guidelines.

Alzheimer's disease

Genes linked to inherited Alzheimer's disease. PSEN1 and PSEN2 cause rare early-onset forms, while APOE affects risk for the more common late-onset form.

Parkinson's disease

Genes tied to typical-onset Parkinson's disease. LRRK2 and GBA are the most common genetic risk factors and are actively being targeted by new therapies.

Young-onset Parkinson's & parkinsonism

Genes behind Parkinson's that starts before age 50. These tend to be recessive (inherited from both parents) and often progress more slowly.

Frontotemporal dementia & ALS overlap

Genes behind frontotemporal dementia (FTD), which affects personality and language. C9orf72 can cause both FTD and ALS in the same family.

Rare movement & dystonia disorders

Genes causing inherited dystonia and movement disorders. Some, like GCH1, respond very well to medication when diagnosed.

Rare inherited dementias

Genes behind rare forms of inherited dementia, including prion disease, CADASIL (small vessel strokes), and white matter disorders.

Trusted by Thousands

What customers say

Real results from real people taking control of their brain health.

★★★★★

“Turned my family history into a real action plan”

Linda M.58

★★★★★

“Knowing my LRRK2 status gave me a head start”

Robert C.52

★★★★★

“Now my whole family has a prevention roadmap”

Angela D.41

Take the first step for your brain health

Know your genetic risks. Share with your doctor. Plan ahead with confidence.