Type
Blood Testing
Biomarkers
9
Duration
30 min
Results
21 days
Sample
Saliva sample or cheek swab (varies by provider)
What's included
4 deliverables in this treatment
- DNA extraction and analysis
- Genetic variant identification
- Risk assessment report
- Specific genes tested vary by panel
Comprehensive DNA test using saliva to analyze genetic health risks and ancestry.
About this treatment
Genetic health tests analyze your DNA to identify inherited variants that may affect your health risks, medication responses, and nutritional needs. Unlike standard blood tests that measure your current state, genetic tests reveal your underlying predispositions — information that doesn't change over time and only needs to be tested once. Common panels examine variants related to cardiovascular risk (APOE, Factor V Leiden), medication metabolism (pharmacogenomics), methylation (MTHFR), nutrient processing, and disease susceptibility. This information can help personalize your preventive health strategy and medication choices.
Good to know
- Type
- DNA analysis (one-time test)
- Sample
- Saliva or cheek swab
- Turnaround
- 2–4 weeks
- Results
- Lifetime relevance — DNA doesn't change
- Common Use
- Risk assessment, pharmacogenomics
Who is this for?
Anyone interested in personalized health insights based on their genetic makeup. People with a family history of genetic conditions who want to know their carrier status. Those wanting to optimize nutrition and supplementation based on genetic variants (e.g., MTHFR for folate metabolism). Patients who have experienced adverse medication reactions and want pharmacogenomic guidance.
Preparation required
No fasting required. Sample collection is typically a saliva sample or cheek swab — no blood draw needed for most genetic tests. Results take longer than standard blood tests because DNA analysis requires specialized laboratory processing.
Panel categories
Biomarkers tested
9The CBS gene helps turn homocysteine into important substances for our body, like proteins and antioxidants that fight cell damage. Some genetic mutations, like the A13637G variant, can weaken this process, potentially raising homocysteine levels and causing cardiovascular issues.
The V158M mutation in COMT can change how quickly your body breaks down dopamine, adrenaline, and noradrenaline which affects mood, thinking, and stress. This contributes to health outcomes including cognitive performance, susceptibility to psychiatric disorders, and stress-related conditions.
MTHFD1 helps convert one form of folate into another form that is critical for making DNA and RNA, as well as for providing methyl groups for important cellular processes like methylation. Mutations in MTHFD1 result in lower levels of active folate, which is a key input for downstream biological pathways.
MTHFR helps our bodies use folate effectively, but certain genetic differences, like C677T and A1298C, can slow it down. If someone has two copies of C677T or a mix of C677T and A1298C, it slows MTHFR even more, making it harder to convert homocysteine. This could lead to higher homocysteine levels, which might increase the risk of heart problems.
MTHFR helps our bodies use folate effectively, but certain genetic differences, like C677T and A1298C, can slow it down. If someone has two copies of C677T or a mix of C677T and A1298C, it slows MTHFR even more, making it harder to convert homocysteine. This could lead to higher homocysteine levels, which might increase the risk of heart problems.
MTR and MTRR use folate and vitamin B12 to produce a crucial substance called methionine. If someone has two identical mutations in MTRR, or mutations in both MTR and MTRR, it can greatly reduce methionine production, potentially leading to higher levels of homocysteine in the blood and raising the risk of conditions like coronary artery disease.
MTR and MTRR use folate and vitamin B12 to produce a crucial substance called methionine. If someone has two identical mutations in MTRR, or mutations in both MTR and MTRR, it can greatly reduce methionine production, potentially leading to higher levels of homocysteine in the blood and raising the risk of conditions like coronary artery disease.
The PEMT C744G mutation is associated with having lower choline production in the liver. Choline is essential for a neurotransmitter called acetylcholine, which helps send messages through to various organs like the lungs, heart, and brain. If you don't get enough choline, it could affect memory and sleep, as well as how your organs work.
The PEMT M175V mutation is associated with having lower choline production in the liver. Choline is essential for a neurotransmitter called acetylcholine, which helps send messages through to various organs like the lungs, heart, and brain. If you don't get enough choline, it could affect memory and sleep, as well as how your organs work.
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Treatment highlights
- DNA extraction and analysis
- Genetic variant identification
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