About Genomind
Genomind’s at-home test examines selected variants relevant to medication response. An independent clinician authorizes the cheek-swab test, and a genetic counselor helps explain the report. Your prescribing clinician remains responsible for medication choices.
Complete clinician authorizationReturn cheek swabsDiscuss results with a counselor
Offering
Genomind At-Home PGx Test
$599
one-time
Targeted medication-response panel
Includes 30-minute genetic counselor consultation
At-home targeted medication-response genotyping, with included clinician authorization and a genetic-counselor conversation.
What’s included
Included
Genomind Pharmacogenetic Test
*2, *3, *4, *5, *6, *7, *8, *9, *10, *17, *35
*2, *3, *4, gene deletion (*5), gene duplication, *6, *7, *8, *9, *10, *11, *12, *14, *15, *17, *29, *41
*2, *3, *4, *5, *6, *8, *11, *13, *27
*5
*3, *6, *7
Not included
- Hereditary cancer assay scope
- Not included in this PGx-only purchase; no cancer/heart/carrier report assay or variant count applies. Selected PGx genotyping does not supply this report.
- Inherited heart assay scope
- Not included in this PGx-only purchase; no cancer/heart/carrier report assay or variant count applies. Selected PGx genotyping does not supply this report.
- Carrier screening assay scope
- Not included in this PGx-only purchase; no cancer/heart/carrier report assay or variant count applies. Selected PGx genotyping does not supply this report.
Before you buy
- Before collecting
- Follow the supplied collection instructions. The lab must receive your sample within three months of the order.
Results
Report
The report explains gene-related medication effects and provides information to discuss with a prescriber.
Official sample- Results
- Medication-related genetic findings to download and share with your prescriber.
- Access
- Web
- Download
- Downloadable reports
- Timing
- Typically 1–2 weeks overall; help estimates 2–3 business days after the lab receives the sample. Shipping, authorization and counselor availability affect the overall interval.
Help
Live consultation
IncludedA genetic counselor explains your results in a 30-minute virtual appointment, with medication changes handled by your own prescriber.
Collection
Complete independent authorization, collect cheek swabs at home and use the prepaid mailer. Genetic counseling follows the report.
Reviews
What people praise
Reports to discuss with your clinician
Customers value receiving detailed information to discuss with their clinician; some specifically describe their doctor helping them understand the report and what it means for their care.
What people complain about
Unexpected bills and payment disputes
Some customers describe bills that differ from their initial expectations, including additional charges after paying upfront or lengthy exchanges about insurance payments and remaining balances.
Stories
Virginia von Rhine
A new direction after years of unsuccessful treatment
Virginia had tried many antidepressants without finding lasting relief. Genomind testing gave her clinician additional information for a different treatment plan; she told WHYY that the change helped her feel motivated to get out of bed and do things again.
whyy.orgLarry Bone
Fewer migraines after a medication review
Larry had struggled with severe migraines and difficult medication reactions for decades. His doctor used Genomind results alongside clinical judgment to change his prescriptions, and Larry reported only two minor attacks over the following ten months.
genomind.comThings to know
- Return the kit within three months.
Postshipment cancellation deductions and refund limits apply.
- Authorization and counseling are included.
The self-pay test includes authorization and a genetic-counselor appointment; medicines and prescribing care are separate.
- Optional sample storage has separate consent.
De-identified research and service processing are permitted; optional leftover-sample research storage has separate consent.
- Independent authorization is included.
The home route requires US eligibility and an independent clinician’s approval.
Alternatives
dnaPower · pharmaPower
A medication-response report with optional pharmacist interpretation rather than an included genetic-counselor session.
Est. $321
Dr. Jeffrey Etemad · Mental Wellness
Defined Mental Wellness SNP-interpretation package with its own clinic review.
Est. $1,300
Picture Genetics · PGx
Targeted pharmacogenomic drug-response reports.
$295
Golberg Longevity · Concierge Longevity Membership
The Longevity Diagnostic assessment followed by quarterly reviews and ongoing access to Dr. Golberg.
$3,000/monthFAQs
What does the $599 price include?
The kit, clinician authorization, laboratory testing, reports, shipping/handling and a 30-minute genetic-counselor consultation. There is no required test subscription; prescribing care and medicines are separate.
Will Genomind change my prescriptions?
No. Neither Genomind nor PWNHealth makes prescribing decisions through this purchase. Take the results to the clinician managing your medications.
Can I use insurance for this purchase?
The selected at-home package is self-pay. Insurance-billed PGx testing requires a separate order from your existing clinician; that route can have different financial terms. HSA/FSA payment is advertised, subject to plan rules.
Does it screen for disease risk or ancestry?
No. This is a medication-related genetic report, rather than cancer, inherited-condition, carrier or ancestry screening. The separate Mental Health Map product is not bundled here.
Does it sequence all of these genes?
No. Targeted genotyping tests selected variants and misses unlisted ones. Gene/drug counts do not mean complete-gene coverage or equally actionable results.
When must I return my sample?
The lab must receive it within three months of the order; otherwise the order is canceled without refund. A quality-failure replacement has its own three-month submission window. See the policy for applicable refunds and exceptions.
How do storage and research choices work?
Optional leftover-sample research consent permits indefinite deidentified sample storage/research. The privacy policy separately permits internal deidentified data research and legally required record retention; declining sample storage is not a promise to erase every clinical record.