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Carrier Screening - 15+ Conditions

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Rs. 3,000.00
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Rs. 3,000.00
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Carrier Screening - 15+ Conditions - Mapmygenome
BENEFITS +

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

WHAT'S INCLUDED +

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

SAMPLE TYPE +

  • No sampling required

TESTING TECHNIQUE +

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

Features

  • Personalized and Actionable

  • Pan India Shipping

  • Digital Reports

  • Secure Personal Data

FAQs

Who can benefit from this test ?

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

How do we analyze?

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

How long does it take to get the report?

2 weeks