Cancer is not just an individual disease — it's a family disease. When one family member is diagnosed, the genetic implications ripple outward. Siblings share roughly 50% of their DNA. Children inherit half from each parent. Having the family's genomes stored creates a network of biological data that becomes exponentially more valuable together than individually.
Knowing that your mother carried a BRCA1 mutation is useful information. Having your own genome sequenced to confirm whether you inherited it is actionable information. The difference between knowing family history and knowing your own genomic reality is the difference between worry and clarity.
When a family member develops cancer, comparing their tumor genome against the genomes of healthy family members can reveal inherited mutations that increase risk for everyone. This early identification allows proactive screening and prevention for family members who share the risk.
At $199 per genome, sequencing a family of four costs less than a single emergency room visit. It's an investment in preparedness that protects everyone — and the data never expires.
Related: Cancer Preparedness and Your Genome · Sequencing Costs Less Than Your Phone Bill · View Pricing
Ready to secure your genome?
Join the Waitlist