173 Conditions · 165 Genes · 11,000+ Variants

Understand whether you carry genetic variants that could be passed to your future children—ideally before pregnancy or early in your family-planning journey.

VISTA™ Targeted Panel 2.0 PLUS is a comprehensive carrier screening test covering 173 inherited conditions across 165 genes and more than 11,000 pathogenic variants.

It includes everything in the Mini Panel, plus additional important inherited conditions, making it the panel most couples choose.

Key Benefits

• Screens 173 inherited genetic conditions
• Analyses 165 genes
• Covers more than 11,000 pathogenic variants
• Detection accuracy above 99%
• 99.9% sensitivity
• 99.9% specificity
• Suitable for individuals and couples planning a family
• Helps couples make more informed reproductive decisions

Conditions Include

• Duchenne muscular dystrophy
• Tay-Sachs disease
• Maple syrup urine disease
• G6PD deficiency
• Gaucher disease
• Everything included in the Mini Panel
• Many other inherited genetic conditions

Why Carrier Screening Matters

A healthy person can carry a genetic condition without experiencing any symptoms or knowing it runs in the family.

If both partners carry variants associated with the same recessive condition, their child may have an increased chance of inheriting that condition. Screening can identify this possibility before pregnancy or early enough to discuss available options with a qualified healthcare professional.

Who Should Consider This Test?

• Couples planning a pregnancy
• Individuals who want to understand their carrier status
• Couples with a family history of inherited conditions
• People undergoing fertility treatment
• Couples from the same or closely related ethnic background
• Anyone seeking broader screening than a basic carrier panel

Easy E-Voucher Process

1. Purchase your e-voucher today.
2. Book at least six hours before your visit through WhatsApp, LINE or email.
3. Visit the MedEx clinic within 180 days of payment.
4. Provide the required sample as instructed.
5. Receive your carrier screening report when available.
6. Review significant findings with a qualified healthcare professional.

E-Voucher Details

• Validity: 180 days from payment
• Coverage: 173 conditions and 165 genes
• Variants: More than 11,000 pathogenic variants
• Booking: At least six hours in advance
• Booking channels: WhatsApp, LINE or email
• Sample: Collection instructions will be provided
• Preparation: Instructions provided after booking

Plan your family journey with more information and greater confidence. Purchase your e-voucher today and complete the test anytime within 180 days.

Carrier screening estimates the chance of carrying selected genetic variants. It does not test for every genetic condition, guarantee a healthy pregnancy or diagnose a condition in a future child. Results should be reviewed with a qualified healthcare professional or genetic counsellor.