Make sense of your DNA

Clear, evidence-backed health insights from your DNA file, without the black box.

  • Upload raw data from SNP arrays, WGS, or WES.
  • See genes, variants, pathways, medication-response notes, and the evidence behind them.
  • Designed to help you understand your DNA, not replace medical advice.

By the numbers

Turn raw DNA data into readable health context

Gene Inspector combines ready-made health panels with deeper variant review, so you can move from a broad topic to the evidence behind a finding.

23,605 genes in the database

Annotated and explained so you can review genes without decoding raw database fields.

102 Prebuilt panels

Vitamins, minerals, hormones, medication response, and essential pathways. Create your own panels too.

8 Predictors

Help surface SNPs and mutations that may deserve closer review.

Generated product illustration of DNA and medication evidence cards
Medication response See how genetic variants may affect medication response and where the evidence comes from.

Pharmacogenomics

How genes may change medication response

Genetic variants can influence how the body processes or reacts to medication. Gene Inspector finds the relevant medication notes in the uploaded DNA file and shows the details behind them.

28,139 medication-response notes
1,165 medications covered
8,431 research references
Example TNFRSF11A rs1805034
CT
frequency 0.55

Toxicity Patients with the CT genotype who are treated with acetaminophen, aspirin, diclofenac, propionic acid derivatives or Pyrazolones may have an increased risk of urticaria and Angioedema as compared to patients with the TT genotype. Other genetic and clinical factors may also influence a patient's risk for urticaria and Angioedema.

Want to see the product before uploading anything? Explore Demo Genome

Prebuilt panels

Start with what you're curious about

Use ready-made panels for common topics, then create your own when something else catches your attention.

Common starting points Panels are just the starting point. You can explore any gene or variant in your file.
102 prebuilt panels

Vitamins

Panels for genes that synthesize, activate, transport, or use vitamins.

14 panels
  • Vitamin A
  • Thiamine (B1)
  • Riboflavin (B2)
  • NAD (B3)
  • Pantothenic acid (B5)
  • Pyridoxal Phosphate (B6)
  • Biotin (B7)
  • Folate (B9)
  • Cobalamin (B12)
  • Vitamin C
  • Vitamin D
  • Vitamin E
  • Vitamin K
  • Vitamin Q (Queuosine)

Minerals

Panels for mineral metabolism, transport, use, and trace-metal balance.

12 panels
  • Iron (Fe)
  • Copper (Cu)
  • Selenoproteins
  • Molybdenum
  • Sulfur (S)
  • Zinc (Zn)
  • Magnesium (Mg)
  • Iodine (I)
  • Manganese (Mn)
  • Calcium (Ca)
  • Phosphate (P)
  • Electrolytes (Na/K/Cl)

Hormones

Panels for synthesis, release, transport, receptor signaling, conversion, and clearance.

22 panels
  • Thyroid
  • Estrogen
  • Androgens
  • Progesterone
  • Cortisol
  • Aldosterone
  • Catecholamines
  • Melatonin
  • Insulin / Glucagon
  • GH / IGF Axis
  • Prolactin
  • Gonadotropins
  • Vasopressin / Oxytocin
  • Calciotropic Hormones
  • Gut Hormones
  • Adipokines / Appetite
  • Cardiorenal Peptides
  • Hematopoietic Hormones
  • Placental Hormones
  • Relaxin / INSL Peptides
  • Melanocortin / Orexin
  • Endocrine FGFs

Energy & pathways

Panels for core metabolic routes that generate and manage cellular energy.

8 panels
  • Mitochondrial DNA
  • Krebs cycle (TCA)
  • Fatty Acids Oxidation
  • Ketones
  • Gluconeogenesis
  • Branched-Chain Amino Acids
  • Pentose Phosphate Pathway
  • Urea cycle

Supporting pathways

Panels for systems that influence detoxification, antioxidant defense, transport, and signaling.

18 panels
  • Glutathione
  • Heme
  • Coenzyme Q10
  • Creatine
  • Glycine
  • Histamine
  • PLP-dependent enzymes
  • Circadian rhythm
  • Endocannabinoid System
  • Apolipoproteins
  • PPARs
  • NRF2
  • PI3K-Akt-GSK3b
  • Autophagy
  • Transporters
  • Immune system
  • Oxalates
  • AMPD1 Network

Genetic disorder collections

Panel collections for rare disease, metabolic disorder, neurological, connective tissue, and endocrine questions.

20 panels
  • Lysosomal Storage Disorders
  • Neuromuscular Disorders
  • Mitochondrial disorders
  • Hyperammonemia
  • Glycogen storage disease
  • Hyperinsulinism
  • Acidurias
  • Porphyrias
  • NBIA
  • Maple Syrup Urine Disease
  • Mucopolysaccharidosis
  • Bleeding Disorders
  • Ehlers-Danlos syndrome
  • MCAS
  • Polycystic Ovary Syndrome
  • Kidney stone disease (monogenic)
  • Hirsutism
  • Seizures
  • ME/CFS
  • Other Rare Diseases
Custom panels Create your own lens when the question does not fit a predefined panel.
Explore panel examples in the demo genome. Explore Demo Genome

Evidence view

See the evidence behind each DNA finding

Open a gene or variant to see what was found, why it may matter, which sources support it, and what you want to research next.

Try the evidence view with sample data. Explore Demo Genome

Pricing

Choose your plan

Start with one genome. A practitioner tier is available when you need more capacity.

For Health Practitioners

Starting from

$99/month
  • Work with up to 15 active genomes.
  • Unlimited archived genomes.
  • Cancel anytime.
Create Practitioner Account
Not ready to choose a plan? Start with the free demo. Explore Demo Genome

Responsible use

Research and educational use only

Gene Inspector Pro provides non-clinical information for research, education, and general wellness review. The service is not reviewed, cleared, or approved by the FDA, and it does not diagnose, treat, prevent, mitigate, or cure any disease, condition, or disorder.

Consultations or third-party professionals connected with Gene Inspector Pro do not provide medical opinions, clinical assessments, healthcare services, or any regulated professional care through the service. No physician-patient or licensed provider-patient relationship is created.

Information from the service is not a substitute for professional medical advice, diagnosis, or treatment. Consult a licensed physician or qualified healthcare provider before making health-related decisions, especially if you have or suspect a medical condition. Please use this information as part of your own research and in consultation with your healthcare provider.