One time genetic screening

Scan X+

Scan X+ combines full-body imaging, advanced biomarkers, and deep genetic analysis to give the most complete view of your current and inherited health risks. With MRI, CT Calcium Score, DEXA, ECG, 100+ biomarkers, PRS, and NGS, it merges your scan, blood, and DNA data into an AI-driven, doctor-reviewed plan for precision prevention and longevity

₹50,000

₹25,000 + ₹25,000

With one time for genetics

₹50,000

₹25K + ₹25K

₹25,000 is for one-time genetics screening

What you get with Scan X+

Features of the Scan X+

Genetic Risk Mapping for Heart, Brain, Cancer, and Metabolic Health

For many major diseases like heart disease, diabetes, and some cancers, genetics can explain a large share of your risk often 30–60%. Genetic Risk Mapping helps you understand that inherited part of your risk

NGS and PRS for Hereditary Cancer and Cardiac Genes

Sequence of high-impact genes associated with hereditary cancer and cardiac syndromes, and analyse hundreds of thousands of genetic markers for polygenic risk scores in heart and metabolic disease

Comprehensive Early Cancer Detection

Full-body MRI detects tumors and abnormalities early across organs and without radiation. It reveals cancers and neurological issues long before symptoms appear.

Heart Health, Deeply Analyzed

Ultra-low dose CT Calcium Scoring + ECG assess plaque buildup and heart rhythm enabling early, preventive detection of heart disease and cardiovascular risk

Bone Strength & Advanced Metabolic Health analysis

DEXA scan to measure bone density, muscle mass, and visceral fat essential for assessing osteoporosis, metabolic risk, body composition, and long-term musculoskeletal health

200+ Condition Risk Detection

Early warning signs of 200+ major diseases — from neurodegeneration to chronic inflammation. Combines biomarkers and imaging to detect risks long before symptoms emerge

Extensive analysis with 100+ parameters

Cover everything from essential nutrients to vital organ functions, these tests provide a detailed snapshot of your overall wellness.

Get a comprehensive health score along with organ wise scores as well

Discover your overall health score, a single number that reflects your general well-being. Dive deeper into organ-wise scores for detailed insights into specific areas of your body's performance.

Personalized Recommendations

From dietary adjustments to exercise routines and sleep optimisation, every suggestion is personalised to help you achieve your goals.

1-1 consultation with an expert

One-on-one consultation from a specialist who reviews your results in detail.Get clear, actionable guidance on your risks and imbalances

What all gets covered?

Decode Your DNA

Research shows genetics can account for 30–60% of your risk for major diseases like heart disease, diabetes, and some cancers. We decode your your genes using advanced NGS and PRS to reveal silent risks

Cancer

The Cancer panel screens for hereditary predispositions across multiple organs - including breast, ovarian, prostate, colon, pancreatic, endometrial, kidney, skin, thyroid, and brain cancers.

Heart Health

We detect risk for Coronary Artery Disease (CAD), Cardiomyopathies (Hypertrophic, Dilated, Arrhythmogenic), Arrhythmias , and Familial Hypercholesterolemia.

Brain Health

The neuro module focuses on detecting genetic susceptibility to Alzheimer's and Parkinson's disease using PRS and select NGS variants.

Metabolic Health

This module evaluates your genetic tendency for metabolic disorders like Type 2 Diabetes, Obesity, Hypertension, and High Cholesterol.

How Cent AI genetic testing works

The Science Behind Your Genetic Risk

We use NGS to analyse 60+ high-impact genes and PRS to assess hundreds of thousands of markers. Built on large South Asian datasets, our models deliver accurate, population-specific insights

Understanding the Two Layers of Genetic Risk

We assess your genetic health using two complementary methods: Next Generation Sequencing (NGS) and Polygenic Risk Scoring (PRS).

NGS

Some monogenic diseases are caused by a single gene carrying a strong mutation. NGS scans clinically important genes to detect these high-impact variants

PRS

Many common conditions are by thousands of tiny genetic variations. PRS analyses hundreds of thousands of genome-wide markers to calculate your overall inherited tendency toward these diseases.

Cent AI’s Preventive genomic assessment combines NGS and PRS. By analysing these two layers of genetic information, tailored to South Asian datasets, CENT AI provides a clearer understanding of your risks for heart disease, diabetes, cancers, brain conditions, and more. These insights help you make informed decisions about lifestyle, screening, and long-term health planning.

FAQ

Frequently Asked Questions

Scan X+ combines full-body MRI, low-dose CT calcium scoring, DEXA, 100+ biomarkers, and PRS + NGS genetic analysis. It detects 200+ diseases, including cancer, heart, neuro, metabolic, and genetic disorders — years before symptoms.

Scans detect present abnormalities, but genetics detects future risk — allowing you to act years before symptoms. PRS & NGS reveal your risk for:

Heart disease

Cancer (breast, colorectal, ovarian, prostate)

Alzheimer’s & neurodegeneration

Diabetes & metabolic syndrome

We use PRS (Polygenic Risk Score) for prediction & NGS (Next Generation Sequencing) for gene-level mutations. Together, they provide the most complete genetic risk report available in India.

Yes. That’s the core purpose. Scan X+ detects existing diseases + future genetic risk, allowing preventive action years in advance.