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Genetic
Whole Genome Sequencing
Comprehensive analysis of your entire ~3 billion base pair genome — the most complete genetic test available.
Optimal Range
Identification of pathogenic variants and risk alleles
Why It Matters
WGS identifies inherited risks for cancer (BRCA1/2, Lynch syndrome), heart disease (familial hypercholesterolemia), and neurodegenerative conditions. It also reveals longevity-associated variants in genes like FOXO3 and SIRT1, enabling truly personalized prevention.