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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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.

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