Carrier Screening for India

Know your carrier status before starting a family. GenAssure offers comprehensive exome-based carrier screening for inherited conditions prevalent in the Indian population.

NABL Accredited (ISO 15189:2022) PC-PNDT Approved CGHS Empanelled

10,000+

Screenings

200+

Conditions

99.9%

Accuracy

Pan-India

Coverage

How It Works

Three simple steps from order to results.

Step 1

Order Your Test

Create an account, place your order, and pay securely via Razorpay.

Step 2

Sample Collection

Receive a collection kit at your doorstep. Provide a simple blood sample.

Step 3

Get Results

Receive a detailed carrier screening report with genetic counseling guidance.

All Tests

Included with every GenAssure product

Disease Predisposition

Identify pathogenic variants linked to hereditary conditions with ACMG-classified clinical significance.

Pharmacogenomics

Understand how your genes affect drug metabolism. Get personalized medication guidance based on CPIC guidelines.

Ancestry Composition

Discover your genetic heritage with detailed population breakdowns and migration history.

Maternal Lineage

Trace your maternal ancestry through mitochondrial DNA haplogroup analysis spanning thousands of years.

Carrier Screening

Couple screening for autosomal recessive conditions. Plan your family with genetic confidence.

Variant Explorer

Research-grade variant browser with ClinVar, gnomAD, and VEP annotations for deep exploration.

Who We Serve

Built for every stakeholder in the carrier screening journey.

Consumers

Individuals and couples planning a family. Order directly and pay online — get clarity about your carrier status from home.

Get Started

Clinical Labs

Partner labs that collect samples and need a comprehensive sequencing and reporting pipeline with full LIMS integration.

Partner With Us

Clinics

OB-GYN and genetic counseling clinics offering carrier screening to patients, with white-label reporting options.

Learn More

Why GenAssure

Purpose-built for India's carrier screening needs.

Exome-Level Depth

Comprehensive exome sequencing captures variants that targeted panels miss.

FHIR-Compliant Workflow

Interoperable clinical data from sample to report, following global standards.

India-Focused Panel

Curated for conditions prevalent in the Indian population, not a one-size-fits-all import.

Secure & Private

End-to-end encryption, consent-based data handling, and full audit trails.

Ready to know your carrier status?

Get started today and take the first step toward informed family planning.

Get Started