Every test has one self-pay price, paid when you order. Insurance billing for GenePGx is coming soon.
Genotyped in our own CLIA-certified lab (New York orders excepted)
Your genetic data is never sold, and never shared for marketing or research
Reports are yours to keep
Full refund within 30 days of ordering, as long as your results haven’t been delivered.
The sample
Oneperson.Threetests.
A sample report for a made-up person, from three tests. Move between its sections; every row and result is made up.
1 · Your summary2 · What each result means3 · What to discuss with your clinician
IllustrativeIllustrative, not a real person’s result
1
GeneMatrix report · Sample
A. Rivera
A made-up person.
Three tests in this sample
Tests
GenePGx · GeneCancer · GeneDiet
Results
3 medication · hereditary cancer · 3 wellness
GenePGx · Medication response
Three results shown
CYP2C19Intermediate metabolizer
CYP2D6Normal metabolizer
SLCO1B1Decreased function
2
CYP2C19 *1/*2
Intermediate metabolizer
Poor
Intermediate (this result)
Normal
Rapid
Ultrarapid
3
Guidance exists for
clopidogrel, citalopram, sertraline
CYP2D6 *1/*1
Normal metabolizer
Poor
Intermediate
Normal (this result)
Ultrarapid
Guidance exists for
codeine, tramadol, ondansetron
SLCO1B1 rs4149056 T/C
Decreased function
Poor
Decreased (this result)
Normal
Increased
Guidance exists for
simvastatin, atorvastatin
Pharmacogenomic results describe how your body is likely to process certain medicines. They do not tell you whether a medicine will work for you, and they are not dosing instructions. Never start, stop or change a medication because of a genetic result. Bring it to the prescriber who manages your medicines.
This view comes from GenePGx · $399, self-pay price
None of the pathogenic or likely pathogenic variants tested was detected.
What it means
None of the variants this panel tests for was found. The panel does not read every position in these genes, so a variant it does not test for may still be present.
3
Next step
Keep to the screening your doctor recommends, and bring this report to your next appointment.
What it can’t find
Variants that are not on its list. That includes most rare variants, and new ones not yet described.
Large deletions or duplications, where a whole section of a gene is missing or repeated.
So a result with nothing found does not rule out an inherited cancer risk.
Testing for inherited cancer risk is a screening test, not a diagnosis. A result with no variant found does not mean you will not develop cancer, and finding a variant does not mean you will. Talk to your doctor or a genetic counselor before making any decision about screening, medication or surgery.
This view comes from GeneCancer · $399, self-pay priceSelected variants only, by genotyping. Not a full-gene test.
WellnessFor general wellness and information, not diagnosis.
GeneDiet · Nutrition traits
Three traits shown
Caffeine: Faster
Lactose: Persistent
Appetite and fullness: Typical
2
Caffeine
Associated with clearing caffeine more quickly than is typical, across groups studied.
Slower
Typical
Faster (this result)
Lactose
Associated with digesting milk sugar into adulthood.
Non-persistent
Persistent (this result)
Appetite and fullness
Associated with typical hunger and fullness signals across groups studied.
Lower
Typical (this result)
Higher
The associations come from population studies and describe tendencies across groups, not how any one person responds. Our nutrition, supplement, athletic and wellbeing reports are for general wellness and information. The evidence behind these associations is less established than for our clinical panels, and these reports are not intended to diagnose, treat, cure or prevent any disease.
Selected variants, by genotyping: not every position in a gene, and not a whole genome. A variant a panel does not test for may still be present.
Where samples are tested
Our own CLIA-certified laboratory (CLIA 14D2276402). Orders shipped to New York are completed through a physician order or a reference laboratory permitted in New York.
This sample
The person and every result here are made up. A real report sets out your own results, for the tests you choose.
Our genetic tests are laboratory-developed tests performed in our own CLIA-certified laboratory. New York is the exception: orders shipped there are completed through a physician order or a reference laboratory permitted in New York. Our genetic tests have not been cleared or approved by the FDA. Results describe inherited traits and risks and are meant to inform decisions you make with your clinician. They are not a diagnosis.
IllustrativeIllustrative, not a real person’s result
GenePGx · Medication response
1
The result
What was found, in plain words, before any detail.
CYP2C19 *1/*2
Intermediate metabolizer
2
Where it sits
The range of possible results for this gene, and this one on it.
Poor
Intermediate (this result)
Normal
Rapid
Ultrarapid
3
Guidance exists for
Medicines with published guidance for this gene. It is not advice about them.
clopidogrel, citalopram, sertraline
4
The note
What a medication result can and cannot tell you.
Pharmacogenomic results describe how your body is likely to process certain medicines. They do not tell you whether a medicine will work for you, and they are not dosing instructions. Never start, stop or change a medication because of a genetic result. Bring it to the prescriber who manages your medicines.
How to read a result
Thehardestview,infourparts.
A medication result says what was found and where it sits on the range of possible results, then names the medicines with published guidance for it. The note beside it says what it cannot tell you.
What this sample shows
01The coverWho it is for, the tests included and a count of results.
02The resultsOne section per test, each result stated first.
03The notesThe plain note each kind of result carries, beside it.
04Methods and limitsWhat genotyping reads, and what it leaves out.
Notes for the appointment
Made-up example
Medication responseIs any of this relevant to the medicines I take now?
Hereditary cancerDoes my family history change the screening you would recommend?
For my recordsWhich of these results should go in my notes?
Take it to your clinician
Areportisthestartofaconversation.
Results describe inherited traits and risks. They are there to inform the decisions you make with your clinician, not to make them for you.
01Read it at homeTake your time. Each result is set out in plain words, with its note beside it.
02Note your questionsMark what surprised you, and what you would like explained.
03Bring it to your appointmentYour clinician can weigh a result against your history and your family. For a medication result, that is the prescriber who manages your medicines.
With GeneMatrix+
Yourreport,readagain.
Your genome doesn’t change. With GeneMatrix+, your reports are re-read automatically whenever the evidence from our sources is updated.
What you send
Nothing more. Each sample is collected once.
If you cancel
Every report stays yours. Re-reads stop when GeneMatrix+ ends.
The first year of GeneMatrix+ is included when you turn on automatic renewal at checkout. After that it’s $99 a year until you cancel. Renewal is charged to your payment method each year. Leave automatic renewal off and you get the test alone, without a GeneMatrix+ year. Cancel anytime online, or by writing to info@genematrix.io. Your reports stay yours.
Ways to buy
Choosehowtogetyourownreport.
Each product line at its own self-pay price, paid once when you order.
Nutrigenomics
$199–$499 one-time$199–$499
One-time payment
GeneCore, the all-in-one, and four single tests. For general wellness.
One-time payment. Self-pay only. We don’t bill insurance for this test. For general wellness and information, not diagnosis.
The first year of GeneMatrix+ is included when you turn on automatic renewal at checkout.After that it’s $99 a year until you cancel. Renewal is charged to your payment method each year. Leave automatic renewal off and you get the test alone, without a GeneMatrix+ year. Cancel anytime online, or by writing to info@genematrix.io. Your reports stay yours.
Pharmacogenomics
$399 self-pay price$399
Self-pay price, paid once
Checks selected known variants in 15 genes, plus CYP2D6 copy number, by genotyping.
One test, GenePGx: how you are likely to process everyday, pain and mental-health medicines.
One price, paid when you order. We don’t send a claim to your health insurance.
The first year of GeneMatrix+ is included when you turn on automatic renewal at checkout.After that it’s $99 a year until you cancel. Renewal is charged to your payment method each year. Leave automatic renewal off and you get the test alone, without a GeneMatrix+ year. Cancel anytime online, or by writing to info@genematrix.io. Your reports stay yours.
Want to use insurance? Insurance billing is coming soon.
Have Medicare, Medicaid or other government coverage? Please contact us before you order.
GeneCancer
$399 self-pay price$399
Self-pay price, paid once
Checks selected variants across 108 genes, including BRCA1 and BRCA2, by genotyping.
If you or a close relative has had cancer, ask your doctor about full-gene clinical testing.
One price, paid when you order. Selected variants only, by genotyping. Not a full-gene test.
The first year of GeneMatrix+ is included when you turn on automatic renewal at checkout.After that it’s $99 a year until you cancel. Renewal is charged to your payment method each year. Leave automatic renewal off and you get the test alone, without a GeneMatrix+ year. Cancel anytime online, or by writing to info@genematrix.io. Your reports stay yours.
Have Medicare, Medicaid, TRICARE or another government health plan? Please contact us before you order.
For families
$399 one-time$399
One-time payment
GeneBaby: inherited conditions screened in a newborn, from a gentle swab along your baby’s gums.
One-time payment. Self-pay only. We don’t bill insurance for this test.
The first year of GeneMatrix+ is included when you turn on automatic renewal at checkout.After that it’s $99 a year until you cancel. Renewal is charged to your payment method each year. Leave automatic renewal off and you get the test alone, without a GeneMatrix+ year. Cancel anytime online, or by writing to info@genematrix.io. Your reports stay yours.
At checkout, a parent or legal guardian confirms they are ordering for their baby.
The guaranteeFull refund within 30 days of ordering, as long as your results haven’t been delivered. Once your results are delivered, the guarantee no longer applies.
Your dataWe never sell your genetic data, and we never share it for marketing or research. It goes only to those who complete your order: the laboratory that runs your tests; for an order shipped to New York, the physician or reference laboratory that completes it; and service providers under contract that store your data or prepare your report for us, including Labrynix and SignalPGx, the laboratory-information and reporting software we use. Once we can bill health plans, and only if you choose to bill our pharmacogenomics (PGx) test to yours, your health plan receives what it needs to process that claim, and for no other purpose. Nutrigenomics and oral microbe results never go to a health plan. That holds while GeneMatrix+ is active and after it ends.
Cancel anytimeCancel anytime online, or by writing to info@genematrix.io. Your reports stay yours; re-reads stop when GeneMatrix+ ends.
Every test has one self-pay price, paid when you order. Insurance billing for GenePGx is coming soon.
01.Is this a real person’s result?+
No. Every view on this page is illustrative, built to show how a report reads. It is not a real person’s result.
02.Will my own report look like this?+
The views here are built to show the kind of information a report sets out. Your results are your own, and the sections depend on the tests you choose.
03.How long until I get my report?+
Results are usually ready 5 to 7 business days after the lab receives your activated sample (10 to 14 business days during holiday weeks). When your results are ready we email you (the email never names your test) with the lab’s secure link to your report, which asks for the tested person’s details before it opens.
04.What does it mean when no variant is found?+
That none of the variants the test looks for was found. Genotyping reads selected variants, so one it does not look for may still be present. Testing for inherited cancer risk is a screening test, not a diagnosis. A result with no variant found does not mean you will not develop cancer, and finding a variant does not mean you will. Talk to your doctor or a genetic counselor before making any decision about screening, medication or surgery.
05.Is this a diagnosis?+
Our genetic tests are laboratory-developed tests performed in our own CLIA-certified laboratory. New York is the exception: orders shipped there are completed through a physician order or a reference laboratory permitted in New York. Our genetic tests have not been cleared or approved by the FDA. Results describe inherited traits and risks and are meant to inform decisions you make with your clinician. They are not a diagnosis.
06.What is the guarantee?+
Full refund within 30 days of ordering, as long as your results haven’t been delivered. Once your results are delivered, the guarantee no longer applies.
Please read
LabOur genetic tests are laboratory-developed tests performed in our own CLIA-certified laboratory. New York is the exception: orders shipped there are completed through a physician order or a reference laboratory permitted in New York. Our genetic tests have not been cleared or approved by the FDA. Results describe inherited traits and risks and are meant to inform decisions you make with your clinician. They are not a diagnosis.
PGxPharmacogenomic results describe how your body is likely to process certain medicines. They do not tell you whether a medicine will work for you, and they are not dosing instructions. Never start, stop or change a medication because of a genetic result. Bring it to the prescriber who manages your medicines.
CancerTesting for inherited cancer risk is a screening test, not a diagnosis. A result with no variant found does not mean you will not develop cancer, and finding a variant does not mean you will. Talk to your doctor or a genetic counselor before making any decision about screening, medication or surgery.
NewbornGeneBaby does not replace the newborn screening your state performs at birth, and it is not a diagnostic test. Deciding to test a child is a decision to make with your pediatrician.
WellnessOur nutrition, supplement, athletic and wellbeing reports are for general wellness and information. The evidence behind these associations is less established than for our clinical panels, and these reports are not intended to diagnose, treat, cure or prevent any disease.
