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MyGevity Plus & AGE
Sale price
$775.00
Regular price
$998.00
Advanced Genetic Insights + Your True Biological Age
Unlock a deeper understanding of your health with two comprehensive at-home tests. The Plus DNA Kit delivers advanced genetic analysis—expanded methylation pathways, hormone dynamics, bone health, and disease risk markers—while the Age Epigenetic Test reveals how fast you're aging at the cellular level. Together, they provide the insights you need to optimize your health and longevity strategy.
What's Included:
Plus DNA Kit
24 reports and 72 tests with polygenic analysis covering:
- Expanded DNA Methylation – MTHFR, MTR, MTRR, COMT, and choline pathways
- Inflammation & Immune Health – CRP genetics, NRF2, chemical/pesticide/BPA sensitivity
- Heart Health – Lp(a) risk, APOe status, atrial fibrillation, CAD risk, hypertension
- Brain Health – Alzheimer's risk (APOE + multi-gene), MCI propensity, stress response
- Hormone Health – Testosterone, estrogen, progesterone, cortisol, thyroid, DHEA-S
- Nutrition & Diet – Saturated fat response, insulin resistance, leptin, food sensitivities
- Vitamin Needs – Vitamin D absorption, B6/B9/B12, nitric oxide production
- Bone Health – Bone density, fracture risk (hip, wrist, lumbar), calcium propensity
- Sleep Health – Deep sleep quality, ideal sleep window
Age Epigenetic Test
The most advanced biological age test available, analyzing 900,000+ DNA methylation sites:
- Biological Age (OMICmAge) – Your true cellular age vs. calendar age
- Pace of Aging (DunedinPACE) – How fast you're aging per year
- 11 Organ System Ages – Heart, brain, liver, kidneys, lungs, immune & more
- Telomere Length – Cellular aging and longevity indicator
- Inflammation Score – CRP & IL-6 chronic inflammation levels
- Immune Cell Analysis – 12-type breakdown of immune function
- Lifestyle Impact Scores – Smoking & alcohol effects on your DNA
Kit Contents:
Plus DNA Kit: Cheek swab tool, stabilization tube, return shipping label, setup guide
Age Epigenetic Kit: Finger-prick lancet, blood collection card, return shipping label, instructions
CLIA Certified Labs
Data Never Sold
GDPR Compliant
Why Bundle These Tests?
Hormone imbalances in your genes?
See how they're affecting your metabolic age.
Expanded methylation variants (MTHFR, COMT, MTR)?
Track their real-world impact on your pace of aging.
Genetic bone density risks?
Check if your skeletal system is aging faster than expected.
Alzheimer's risk markers?
Monitor your brain's biological age over time.
Make changes, retest Age later
Measure the real impact of your interventions.
HIPAA Compliant
GDPR Compliant
At-Home Testing
Data Never Sold
CLIA Certified Labs
Real-Time Tracking
Resources and References
Study 1
DunedinPACE
Title:
DunedinPACE, a DNA methylation biomarker of the pace of aging
Journal:
eLife, Volume 11, e73420, (2022)
Summary:
A 2022 Columbia/Duke study developed DunedinPACE, a blood-based DNA methylation test that measures how fast a person is biologically aging. Validated across 50+ cohorts worldwide, it showed strong associations with morbidity, disability, and mortality — supporting the scientific validity of biological age testing.
Study 2
Using Genomic Information to Guide Weight Management
Title:
NIH Working Group Report — Using Genomic Information to Guide Weight Management: From Universal to Precision Treatment
Journal:
Obesity (Silver Spring), Volume 24, Issue 1, pages 14–22, (2016)
Summary:
An official NIH trans-agency working group — drawing on researchers from Stanford, Mount Sinai, Harvard, Brown University, and the National Cancer Institute — formally established the scientific case for using genomic data to personalize weight management. The report concluded that elucidating the molecular basis of individual variability in weight change has the potential to improve treatment outcomes, and called for moving from one-size-fits-all approaches toward precision, genomics-informed interventions.
Study 3
Measuring biological age
Title:
Measuring biological age using omics data
Journal:
Nature Reviews Genetics, Volume 23, Issue 12, pages 715–727, (2022)
Summary:
Stanford University researchers from the Wu Tsai Neurosciences Institute and Glenn Center for the Biology of Ageing reviewed how omics technologies — epigenomics, transcriptomics, proteomics, and metabolomics — can be harnessed with machine learning to build aging clocks that quantify biological age at the molecular level. Published in Nature Reviews Genetics, one of the most prestigious journals in science, this work establishes the foundational scientific case for why measuring biological age is both possible and clinically meaningful.
Study 4
Genetics of Human Longevity
Title:
The Contextualized Genetics of Human Longevity: JACC Focus Seminar
Journal:
Journal of the American College of Cardiology, Volume 75, Issue 21, pages 2693–2705, (2020)
Summary:
Published in the Journal of the American College of Cardiology — one of the most prestigious cardiovascular journals in medicine — this seminar from the University of Bologna uses centenarians as a scientific model to establish that longevity genes and cardiovascular disease genes are deeply interconnected, representing two sides of the same coin. The authors demonstrate that genetic risk is highly context-dependent, shifting with age, environment, and geography, and that the same allele can be protective or harmful depending on genomic context. Their central argument — that genome-environment interactions must be understood to interpret any individual's disease risk — directly supports the value of comprehensive, personalized DNA profiling.
Study 5
Omics biological ageing clocks and disease risk
Title:
A catalogue of omics biological ageing clocks reveals substantial commonality and associations with disease risk
Journal:
Aging (Albany NY), Volume 14, Issue 2, pages 623–659, (2022)
Summary:
University of Edinburgh and MRC Human Genetics Unit researchers compared 15 different biological aging clocks head-to-head and found that biological age acceleration — when your body ages faster than your calendar age — consistently predicts increased disease risk across multiple conditions. One year of accelerated biological aging carried the same disease risk impact as up to 0.25 additional years of chronological age, with epigenetic clocks among the strongest predictors of generalized aging, confirming that measuring biological age has real and measurable clinical consequences.