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Family Planning (Carrier Status)

Helps you identify genetic variants that could affect your children. With a simple at-home DNA test and detailed report on 40+ conditions, you’ll have the information you need to make confident and informed decisions about your family’s future. View sample report.
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Proven track record: 3+ million analyses delivered

Trusted by 200,000+ users & 2,000+ doctors

Proven track record: 3+ million analyses delivered

Checks for 40+ conditions
Clear, easy-to-understand results
Personalized insights for informed decisions
Convenient at-home testing

Product features

 

Note: To generate your personalized report, purchase a SelfDecode DNA kit. If you already have one, you’re ready to proceed.

 

Are you thinking about starting a family and wondering if there are hidden risks in your DNA that could affect your children? Do you want clarity about whether you might be a carrier of a genetic variant – even if you don’t currently have any health issues? Our Carrier Status Report provides the answers you need in a simple, easy-to-understand format.

 

Understanding Your Carrier Status

With this personalized DNA report, you can learn about key genetic variants that may be passed on and affect a child if both parents carry the same variant. The goal is to give you peace of mind or guide you toward further medical consultation if necessary. By highlighting whether you have a Typical result or if a Variant is Detected, the report offers transparency without unnecessary complexity.

 

What to Expect

Each Carrier Status test focuses on well-defined genetic variants researched for their potential impact on family planning. If you test positive for one of these variants, it does not necessarily mean that your child will inherit the condition – it simply indicates a possibility you’ll want to explore further. For many people, a conversation with a healthcare professional or genetic counselor is the next logical step.

Our carrier status report analyzes your DNA to check for genetic variants associated with over 40 inherited conditions. From common to rare genetic diseases, we provide a comprehensive overview to help you understand potential risks.

 

Tests Included in the Family Planning Report

 

  1. Agenesis of the Corpus Callosum with Peripheral Neuropathy: SLC12A6
  2. Beta-Thalassemia and Related Hemoglobinopathies: HBB
  3. CAD Deficiency: ACADM
  4. Canavan Disease: ASPA
  5. Congenital Disorder of Glycosylation Type 1a (PMM2-CDG): PMM2
  6. Cystic Fibrosis: CFTR
  7. Dihydrolipoamide Dehydrogenase Deficiency: DLD
  8. Familial Dysautonomia: ELP1
  9. Familial Hyperinsulinism (ABCC8-Related): ABCC8
  10. Familial Mediterranean Fever: MEFV
  11. Fanconi Anemia Group C: FANCC
  12. Gaucher Disease Type 1: GBA
  13. Glycogen Storage Disease Type Ia: G6PC1
  14. Glycogen Storage Disease Type Ib: SLC37A4
  15. GRACILE Syndrome: BCS1L
  16. Hereditary Fructose Intolerance: ALDOB
  17. Leigh Syndrome, French Canadian Type: LRPPRC
  18. Limb-Girdle Muscular Dystrophy Type 2D: SGCAM
  19. Limb-Girdle Muscular Dystrophy Type 2E: SGCB
  20. Limb-Girdle Muscular Dystrophy Type 2I: FKRP
  21. Maple Syrup Urine Disease Type 1B: BCKDHB
  22. Mucolipidosis Type IV: MCOLN1
  23. Neuronal Ceroid Lipofuscinosis (CLN5-Related): CLN5
  24. Neuronal Ceroid Lipofuscinosis (PPT1-Related): PPT1
  25. Niemann-Pick Disease Type 1: SMPD1
  26. Pendred Syndrome and DFNB4 Hearing Loss (SLC26A4-Related): SLC26A4
  27. Phenylketonuria and Related Disorders: PAH
  28. Pompe Disease: GAA
  29. Primary Hyperoxaluria Type 2: GRHPR
  30. Pyruvate Kinase Deficiency: PKLR
  31. Rhizomelic Chondrodysplasia Punctata Type 1: PEX7
  32. Salla Disease: SLC17A5
  33. Severe Junctional Epidermolysis Bullosa (LAMB3-Related): LAMB3
  34. Sickle Cell Anemia: HBB
  35. Sjögren-Larsson Syndrome: ALDH3A2
  36. Tay-Sachs Disease: HEXA
  37. Tyrosinemia Type I: FAH
  38. Usher Syndrome Type 1F: PCDH15
  39. Usher Syndrome Type 3: CLRN1
  40. Zellweger Spectrum Disorder (PEX1-Related): PEX1

 

Clear Results and Privacy

Thanks to our straightforward design, there’s no guesswork in interpreting your results. You’ll see precisely whether a variant has been detected or not. And while the report itself doesn’t cover every possible mutation, it delivers a clear snapshot of some of the most relevant genetic markers.

Finally, you can trust that your privacy and data security are taken seriously. This Carrier Status Report complies with both HIPAA and GDPR standards, ensuring that your genetic information remains confidential. Should you have any concerns, you can seek specialized testing or counseling with confidence, knowing you’ve taken the first step in proactive family planning.

WHY SELFDECODE?

Empowering Your Well-being Journey

This personalized health report is powered by SelfDecode's cutting-edge AI technology, designed to unlock a deeper understanding of your health potential. We're committed to providing you with the most accurate and actionable insights to guide your well-being journey.

Most Accurate
Polygenic Risk Scoring

We leverage cutting-edge algorithms and analyze a massive dataset of 2 million people to deliver the most precise assessment of your genetic health predispositions. Our advanced approach takes into account your ancestry - which is often overlooked by other methods - to provide you with the most accurate risk assessment. This ensures that the risk scores you receive are based on the latest scientific evidence and are truly personalized to your genetic makeup.

Cutting-Edge AI &
Machine Learning

We have invested 20 million dollars developing our AI and machine learning models. Our patent-pending technology provides you with the most personalized health insights and recommendations by taking into account your unique DNA, lifestyle, labs, symptoms, conditions and health goals. This empowers you to make informed decisions tailored to your specific needs.

Analyzes 200 Million Variants & Sophisticated Recommendation Engine

We go beyond the basics by analyzing a staggering 200 million genetic variants to provide the most comprehensive picture of your health potential. Our sophisticated recommendation engine leverages this deep analysis to provide personalized and actionable insights to optimize your well-being journey.

Built by Leading
Scientists & Engineers

A dedicated team of over 60 scientists and engineers is continuously innovating and developing our technology, ensuring it remains at the forefront of personalized health.

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  1. Luke

    I purchased the Carrier Reports to understand my risks better. The report flagged my SLC26A4 gene carrier status associated with Pendred syndrome and hearing loss. What I appreciate most is how it explained the gene’s impact without scaring me and provided concrete advice on hearing tests and monitoring. It’s a beautifully organized and scientifically reliable resource.

  2. Kate

    As a mother, I wanted to be sure about passing on any genetic risks. This report identified that I carry a mutation in the SMN1 gene and explained what that could mean for spinal muscular atrophy. The personalized guidance on working with a genetic counselor was invaluable. The visuals and explanations helped me communicate the risks clearly with my doctor and family.

  3. Jeanette

    After years of wondering about genetic conditions in my family, this Carrier Reports answered so many questions. It identified me as a carrier for the PAH gene variant linked to phenylketonuria. The comprehensive explanation and next steps for family planning made it a complete resource. The report is easy to follow even if you’re not a genetics expert.

  4. Vincent

    This report was gold for me as a biohacker. Seeing my specific variants in the HFE and GJB2 genes helped me understand my iron metabolism and hearing issues better. The clear recommendations about monitoring iron levels and avoiding excess noise exposure were very actionable. The graphics simplified complex genetics perfectly. It’s elevated my health strategy significantly.

  5. Thomas

    As someone with a family history of cystic fibrosis, this Carrier Reports was incredibly informative. It detailed my CFTR gene variants clearly and explained the implications for my children’s health. The personalized recommendations for genetic counseling were spot on. This report gave me peace of mind and a practical action plan. Highly recommend for families planning ahead.

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