Heritable Health generates a tier-graded DNA report from your uploaded data, then pairs it with a 30-minute video consultation with a doctor or genetic counsellor. Your consultation focuses on clinically relevant findings today and emerging evidence that may need context.
Every marker we surface carries an evidence tier: STRONG, VALIDATED, MODERATE, EMERGING, or EXPLORATORY. You see what’s clinically actionable today, what’s still under investigation, and where the boundary sits. No false certainty.
Our system generates your DNA report from uploaded data. A doctor or genetic counsellor interprets the report with your goals and family history in mind, including pharmacogenomics, predispositions, and screening considerations that may be relevant to your case.
Where appropriate, we coordinate with your existing healthcare provider and route follow-up testing through suitable local clinical or laboratory pathways. Telegenomics supports ongoing care, but does not replace it.
You see what is clinically actionable today, what is still under investigation, and where the boundary sits. No false certainty.
Direct-to-consumer (DTC) genetic testing provides a broad overview of your genomic profile, yet the clinical interpretation of these findings requires professional oversight. A genetic clinician contextualizes raw data within your personal and family medical history, distinguishing between benign variations and findings that necessitate clinical action.
Professional consultation ensures that your results are understood accurately, mitigating unnecessary anxiety or false reassurance derived from automated reports.
If a report identifies markers associated with hereditary conditions, such as predispositions for cardiovascular disease or oncological risks, clinical follow-up is essential. A qualified professional can determine if additional diagnostic-grade testing is required and assist in developing a proactive surveillance or management strategy tailored to your risk profile.
Heritable Health provides a necessary bridge between raw genetic data and actionable medical guidance. Our goal is to ensure your health decisions are informed by current clinical standards and the latest peer-reviewed genomic research.
We recommend scheduling a consultation if you have identified specific markers of concern or require a comprehensive review of your genetic health profile.
A curated selection from the marker library. Our clinicians can help you interpret what each means in your case.
Bring your raw DNA file. Our clinician reviews it before your call, and the conversation focuses on what’s actionable for you.
Book Your Consultation預約一次初步諮詢並上傳您的DNA數據。
我們的醫師將會審查您的資訊，並可能跟進提出問題。
與醫療專業人士進行一對一通話，以獲取個性化建議和轉介。
遠程基因組學利用遠程醫療提供基因組服務。它包括與遺傳學家的諮詢，以解讀您的基因數據並提供個性化的健康建議。
透過點擊「立即預約諮詢」，您可以透過我們的線上系統預約諮詢。
我們接受來自 23andMe、Ancestry DNA、MyDNA、MyHeritage 和 Family Tree DNA 等測試的 DNA 數據。
是的，我們優先考慮您的隱私和數據安全。所有DNA數據都會安全存儲並以最高的謹慎處理。
Yes, follow-up tests may be recommended after your consultation. Availability, billing, and laboratory pathways depend on your country, region, and healthcare provider.
諮詢透過安全的視頻通話進行，確保個性化和保密的討論。
The human genome is comprised of approximately 6.4 billion base pairs. While the vast majority of our genetic sequence is identical across the species, roughly 10 million positions exhibit variation between individuals. These points of difference represent the biological diversity that influences everything from physical traits to disease susceptibility.
A single nucleotide polymorphism (SNP) is a variation at a specific position in the DNA sequence. As the most prevalent form of genetic variation, SNPs serve as critical biological markers. By identifying patterns in these variations, clinicians can map genetic predispositions and better understand the underlying mechanisms of various health conditions.
