Reports are delivered within 4–8 weeks. Progress updates provided throughout.
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Research that goes where labs don't.
Every service begins with your raw genomic file and your clinical picture. We do not duplicate standard lab reports, we perform advanced research to explore rare, complex, and under-recognized genetic signals.
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OUR SERVICES
Choose your research package
All packages include a physician-ready report with citations, structured for specialist review. Payment plans available at checkout.
Rare Variant Research Report
$399
/one person
For individuals with unresolved symptoms, negative results, or complex presentations.
✓
✓
✓
✓
✓
✓
Deep review of your genome
Identify and investigate key variants
Investigate current research and literature
Assess clinical and biological impact
Build physician-ready cited report
Promote research visibility
Payment plan: 2 monthly payments of $200
Family Research Package
$549
/you + 1 family member
For families where symptoms appear across multiple members.
✓
✓
✓
✓
✓
✓
Everything in Core (both individuals)
Identify and investigate shared variants
Family-based variant analysis and research
Two physician-ready reports
One year variant monitoring
Database submission support
Payment plan: 3 monthly payments of $183
OUR SERVICES
PACKAGES
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Expand your research
Add individual services to an existing package, or as standalone items.
Variant Monitoring
$15
/per month
Ongoing tracking of new research, database updates, reclassifications, and clinical trials specific to your identified variants. Stay informed as science evolves around your case. Annual enrollment is available at $149, a $30 savings over monthly billing.
Additional Family Members
$149
Add a parent, sibling, or child to an existing case for segregation analysis. Comparing variants across family members strengthens the evidence for your doctor, specialist and for research submission.
Consultation
/per family member
We'll help you figure out what you need.
Every case is different. Contact us and describe your situation. We'll recommend the right starting point for your data and your goals.
ADD-ONS
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Custom Research Reports
Targeted genomic research and consultation services for patients, families, and clinicians.
Custom Research
You choose your genomic investigation by biological system or condition. Examples include mitochondrial dysfunction, immune dysregulation, neuromuscular symptoms, medication sensitivities, mental health genetics, chromosomal or sex-linked questions, family planning and more. Pricing based on scope.
Choose Your Research Focus
Genetic Testing Consulting
Genetic Testing Strategy
Not sure where to start? We help you prepare for genetic testing the right way including a concise doctor-ready summary of your symptoms and labs, guidance on physician-ordered vs. direct-to-consumer options, and ensuring you receive the raw genomic data needed for deeper analysis. Testing-and-research packages available.
Clinicians
Clinician Partnership
Structured genomic research support for healthcare professionals managing complex or unresolved cases. We provide case-specific analysis, targeted literature synthesis, and research-aligned reports designed to complement your clinical decision-making.
SPECIALIZED SERVICES
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Two families.
Every year.
Completely Free.
Twice each year, My Variant Coach awards a full genomic research scholarship to a family with a medically complex child who cannot afford advanced genomic analysis.
The scholarship covers comprehensive research for the child and one parent or sibling. This includes full variant analysis, segregation analysis, physician-ready reports, and one year of ongoing monitoring. There is no cost to the family.
Applications are reviewed personally by Myla Fairchild. Recipients are selected based on medical complexity, financial hardship, and the likelihood that deeper genomic research could meaningfully inform the child’s care.
What the scholarship includes
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u
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Full genome variant research for the child
Family-based segregation analysis
Two physician-ready deep research cited reports
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ClinVar submission when appropriate
One year of variant monitoring free
Direct access to Myla throughout the process
Applications are reviewed individually and with care. Email us directly and share your child’s story.