ExoSeq Unlock Comp - افتح المخطط الجيني لصحتك

3,169 درهم

Your DNA could hold the key to every unanswered health mystery you’ve faced. From chronic symptoms to unexplained conditions, many health issues trace back to genetic variations buried deep within your genome. But until now, you’ve only seen the surface. ExoSeq® – Comp opens a new frontier of clarity. By sequencing your full exome—the protein-coding regions of your DNA—it uncovers variants linked to diseases across major medical domains like cardiology, neurology, endocrinology, and gynecology.

نوع العينة: اللعاب (مسحة بوكال)

وقت الدوران: 10–20 Working Days (Upon Lab Arrival)

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ExoSeq Unlock Comp - افتح المخطط الجيني لصحتك
ExoSeq Unlock Comp - افتح المخطط الجيني لصحتك
3,169 درهم
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Your DNA could hold the key to every unanswered health mystery you’ve faced.

From chronic symptoms to unexplained conditions, many health issues trace back to genetic variations buried deep within your genome. But until now, you’ve only seen the surface.

ExoSeq® – Comp opens a new frontier of clarity. By sequencing your full exome—the protein-coding regions of your DNA—it uncovers variants linked to diseases across major medical domains like cardiology, neurology, endocrinology, and gynecology.

Once you explore your genetic map, you’ll discover root causes that may have gone undetected for years. You’ll move beyond treating symptoms and toward understanding the true blueprint of your body.

Imagine working with your doctor using data from your own DNA. It’s not just advanced—it’s transformational. ExoSeq® empowers long-term, personalized health decisions that align with your genetics, not guesswork.

Clinicians and patients worldwide are using ExoSeq® to guide targeted prevention, diagnosis, and treatment. Now it’s your turn.

Key Benefits:

  • Reveals genetic variants across key medical areas – enabling early detection and personalized care

  • Analyzes the protein-coding exome – offering insights tied to real-world health conditions

  • Supports informed clinical decision-making – bridging genomics with medical action

  • Helps uncover underlying causes of symptoms – leading to more precise interventions

Ideal For:

  • Individuals with complex or undiagnosed health conditions

  • Families with hereditary disease risks across specialties

  • People pursuing personalized and preventative medicine

  • Health professionals and patients seeking in-depth genomic analysis

What’s Included?

  • ExoSeq® Comprehensive Test Kit

  • دليل جمع العينات

  • Whole exome sequencing and genetic variant analysis

  • Access to expert consultation for interpretation and next steps

 

نوع العينة: اللعاب (مسحة بوكال)

وقت الدوران: 10–20 Working Days (Upon Lab Arrival)

دليل جمع العينات
مسح رمز الاستجابة السريعة على عدة الخاص بك للوصول إلى دليل خطوة بخطوة. وهو يغطي كل ما تحتاجه لإرسال عينتك إلى مختبرنا ، بما في ذلك المواد وتفاصيل استلام البريد السريع. بعد جمع عينتك ، تأكد من إرسال عينتك في غضون 30 يومًا لضمان المعالجة في الوقت المناسب.

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