DNA Signature – Metabolic Path

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Buccal Swab
Turnaround Time: First test with initial sequencing: 2-3 weeks; All subsequent tests: 48 hours.

Turnaround times are estimates. Detailed order tracking is available in the MosaicDX Portal.

* Available in English

Going Beyond SNPs. Polygenic Risk Scoring for a More Personalized Path Forward.

DNA Signature, a next-generation suite of genomic profiles, looks beyond individual variants, combining polygenic risk scoring with clinical interpretation to translate complex genetics into personalized strategies for better health.

Designed as the genetic companion to the Mosaic Diagnostics Organic Acids Test (OAT), DNA Signature – Metabolic Path evaluates foundational genomic variations governing cellular energy production, nutrient utilization, neurotransmitter balance, gut health, methylation/detoxification, and nutrient needs. By assessing interconnected physiological pathways rather than isolated variants, it provides a comprehensive blueprint of baseline biochemistry to help practitioners uncover the underlying drivers of persistent functional imbalances.

Even when standard biomarkers appear within normal reference ranges, subtle genetic variations can significantly alter metabolic throughput. DNA Signature – Metabolic Path bridges this gap, translating complex genetic data into an actionable clinical strategy for targeted nutrient, dietary, lifestyle, and testing protocols. 

Designed as the genetic companion to the MosaicDX Organic Acids Test (OAT).

For Non-Practitioners:

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What Patients Might Benefit from DNA Signature – Metabolic Path Testing?

Patients with the following symptoms or conditions may benefit from DNA Signature – Metabolic Path testing

  • Unexplained Fatigue & Low Physical Stamina
  • Mood Dysregulation & Low Stress Tolerance
  • GI Complaints & Food/Environmental Sensitivities
  • Seeking Personalized Precision Nutrition & Prevention

Details

Why Use the DNA Signature – Metabolic Path Profile?

Designed as the genetic companion to the Mosaic Diagnostics Organic Acids Test (OAT), DNA Signature – Metabolic Path evaluates foundational genomic variations governing cellular energy production, nutrient utilization, neurotransmitter balance, gut health, methylation/detoxification, and nutrient needs. By assessing interconnected physiological pathways rather than isolated variants, it provides a comprehensive blueprint of baseline biochemistry to help practitioners uncover the underlying drivers of persistent functional imbalances. Even when standard biomarkers appear within normal reference ranges, subtle genetic variations can significantly alter metabolic throughput. The DNA Signature – Metabolic Path bridges this gap, translating complex genetic data into an actionable clinical strategy for targeted nutrient, dietary, lifestyle, and testing protocols.

Our high-complexity laboratory is committed to delivering accurate and reliable results in coordination with these top licensure programs:

Analytes

From a single easy-to-collect buccal swab you will receive a personalized polygenic risk score for the following traits:

  • MTHFR Activity
  • MTR
  • MTRR
  • COMT (Methylation)
  • Phase II Detox Efficiency
  • Vitamin B12
  • Vitamin B6
  • Vitamin B9 (Folate)
  • Vitamin C Propensity
  • Vitamin D Deficiency Risk
  • Iron Deficiency Risk
  • Magnesium Deficiency Risk
  • CoQ10
  • Glutathione
  • Anxiety Propensity
  • Depression Propensity
  • GAD1 Activity
  • OCD Likelihood
  • Rumination
  • Stress Adaptation
  • Stress Phenotype
  • Gut Permeability
  • Mold Sensitivity
  • Oxidative Stress
  • Mitochondrial Function

Sample Reports

The DNA Methylation Profile report aids clinical support for patients by pinpointing SNPs that could potentially impact health and disease risk.

Test Prep and Instructions

MosaicDX offers patient-friendly sample collection kits that simplify testing. Our kits include visual, step-by-step instructions for test preparation and sample collection, personalized shipping cards, and pediatric collection bags if needed. With MosaicDX, patients can easily collect samples for testing with confidence and accuracy.

Frequently Asked Questions

No, we do not. A genetic carrier refers to an individual who has inherited a recessive allele that has been shown to be responsible for an autosomal recessive disease or trait. A genetic carrier only has one recessive allele so while they do not show signs or symptoms of the trait or disease, they are able to pass along the recessive gene to their child.  Our genetic testing is for screening purposes only to assess risk or predisposition for certain traits associated with health and wellness.

No. We do not use patient samples for further research or testing.  We may use your de-identified and anonymized data to help improve our algorithm and reports. Your data will not be sold or shared to or with any 3rd parties/commercial interests.

Yes, we can delete the patient’s raw genetic sequence at any time. Please note that applicable federal and state laws require us to retain your patient report and the subset of your data that was used to generate that report for a specified period of time. We will be happy to delete any and all of your data that we are legally allowed to delete upon request. Please submit your request here.

We implement rigorous selection criteria when choosing which genes or SNPs to include in our panels. The selection and validation criteria are based upon peer-reviewed studies that show a significant association between the SNP variant and trait or condition, the magnitude of the odds ratio (OR) or hazard ratio (HR) to assess risk related to the variant, as well as the population or populations the gene and SNP variant were studied in, the population size, and replication of findings.

A genotype refers to the actual inherited genetic material of an individual that can influence or determine certain characteristics or traits. A phenotype is how the genotype is actually expressed, that is the observable or measurable characteristics or traits of an individual.

SNP is also called a Single Nucleotide Polymorphism. Your DNA consists of 4 main building blocks (nucleotides), Adenine (A), Thymine (T), Guanine (G), and Cytosine (C). In certain locations within your DNA, one person may have an A, whereas another may have a G. This difference in the base pair is often called a variant. This variant is an SNP.

In most situations, you do not have to resubmit a DNA buccal swab sample if you later want to order additional panels. The only time a new DNA buccal swab would need to be resubmitted is if the assay has had significant changes, or the patient previously requested that their DNA sequencing results be deleted.

Patients are sent a DNA Signature Collection Kit containing instructions, 1 cheek swab, a DNA Sample Envelope and a prepaid return envelope and biohazard zip-lock bag. Instructions can also be found on our website on the DNA Signature Profiles web page, along with an easy-to-follow video. 

A person’s polygenic risk score is a statistical calculation based on the presence or absence of multiple genomic variants without taking environmental or other factors into account

Different states have regulations that define the scope of practice for practitioners. It is the practitioner’s responsibility to abide by these rules. Check with your state board of health to determine any restrictions related to laboratory testing. Please note, Mosaic Diagnostics does not offer testing in New York. 

Once you have opened your account, you have the options of ordering kits to stock in your office or drop-ship kits directly to your patients through your MosaicDX portal.   

Watch our short tutorial videos on how to conveniently  

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