Onco Geneguard
Stay Ahead of Cancer with Genetic Clarity
Onco Geneguard
ICMR-NCDIR National Cancer Registry Programme estimates a 12% increase in cancer cases in the country by 2025, approximately 15.7 lakh cases per year.
While lifestyle and environmental factors significantly contribute to cancer risk, genetic variations, particularly single-nucleotide polymorphisms (SNPs), also play a crucial role in individual susceptibility to various cancer types. Understanding these genetic factors can aid in risk assessment, early detection, and personalized treatment strategies.
What Does It Do?
Onco Geneguard evaluates genetic susceptibility to various cancers through SNP analysis. With cancer cases on the rise, it supports early risk assessment, timely detection, and personalized treatment planning.
Polygenic Risk Score (PRS)
A Polygenic Risk Score (PRS) estimates your genetic risk for cancer conditions and traits based on multiple small genetic variants. Unlike single-gene tests, PRS looks at thousands of markers across your genome (GWAS) to provide a more complete risk profile. Each variant contributes a small amount of risk; together, they form your total score. A higher PRS indicates a greater genetic risk for a specific disease compared to the general population
Who Benefits?
Anyone can benefit from Onco GeneGuard, especially individuals with:
With a family history of cancer.
Certain Ethnic Backgrounds known to be at high risk for cancers.
Ones who are Seeking Proactive Health Management.
Core Pillars
Predictive
Understand your inherited risk early
Personalized
Tailor lifestyle or screening plans
Preventive
Take action before symptoms develop
OneDNA Onco Geneguard
Fostering well-being by assessing and managing predisposition of traits, lifestyle diseases and chronic health conditions.
Free Consultation
Speak with our genetic counselors
Technical Specifications
| Specification | Value |
|---|---|
| Technique | Microarray |
| Platform | Illumina Infinium Beadchips-24 BeadChip |
| Bioinformatics Tools | Illumina iScan platform, Genostudio 2.0, SNaPpy 2.0 |
| Coverage | SNP markers including CNVs, Germline Variants, Indels, SNPs, Structural Variants, and sex chromosome markers |
| Accuracy | 99.6% (for classified genes only) |
| Sample Type | Saliva |
| Precautions | Avoid eating or drinking 30 minutes before the test |
Ready to Unlock Your Genetic Insights?
Take control of your health with personalized genetic testing and expert counseling.
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