उत्पाद जानकारी पर जाएं
1 का 1

वाहक जांच - 15+ स्थितियां

नियमित रूप से मूल्य
Rs. 3,000.00
नियमित रूप से मूल्य
विक्रय कीमत
Rs. 3,000.00
शिपिंग की गणना चेकआउट पर की जाएगी।
Carrier Screening - 15+ Conditions - Mapmygenome
फ़ायदे +

Screens for 15+ inherited genetic conditions in a single report
No new sample required — for existing Mapmygenome customers only
Identifies carrier status for serious recessive disorders including cystic fibrosis, sickle cell anemia, and Tay-Sachs disease
Easy-to-understand report with clear explanations of each carrier status
Includes recommendations from certified genetic counselors
Personalized action plan to support informed reproductive decisions
Strict data privacy with bank-level encryption

इसमें क्या शामिल है +

Autosomal Recessive Disorder Panel (15+ conditions)
Carrier Status Summary
Risk Assessment for Offspring
Genetic Counselor Recommendations

नमूना प्रकार +

  • किसी नमूने की आवश्यकता नहीं है

परीक्षण तकनीक +

Carrier screening analysis derived from existing genomic data (Whole Genome Sequencing or equivalent) already on file for the customer. No new sample collection required. Variants are assessed against curated databases of pathogenic and likely pathogenic recessive mutations. Report generated and reviewed by certified genetic counselors.

Screens for 15+ inherited genetic conditions in a single report
No new sample required — for existing Mapmygenome customers only
Identifies carrier status for serious recessive disorders including cystic fibrosis, sickle cell anemia, and Tay-Sachs disease
Easy-to-understand report with clear explanations of each carrier status
Includes recommendations from certified genetic counselors
Personalized action plan to support informed reproductive decisions
Strict data privacy with bank-level encryption

विशेषताएँ

  • वैयक्तिकृत और कार्यान्वयन योग्य

  • अखिल भारतीय शिपिंग

  • डिजिटल रिपोर्ट

  • व्यक्तिगत डेटा सुरक्षित रखें

पूछे जाने वाले प्रश्न

इस परीक्षण से किसे लाभ हो सकता है?

Existing Mapmygenome customers planning to start a family
Couples with a personal or family history of genetic disorders
Individuals seeking preconception genetic risk assessment
Anyone who wants to understand their carrier status before pregnancy

हम विश्लेषण कैसे करते हैं?

Variant analysis from existing Whole Genome Sequencing (WGS) or genomic data on file. No additional sequencing required.

रिपोर्ट प्राप्त होने में कितना समय लगता है?

2 सप्ताह