Built on peer-reviewed evidence, reviewed by clinicians.

Methodology

Our analysis pipeline parses raw genotyping data and cross-references variants against curated public databases including ClinVar, gnomAD, dbSNP, OMIM, and PharmGKB. We prioritise variants with strong, replicated evidence and clear clinical context.

Data sources

• ClinVar — clinically relevant variants
• gnomAD — population allele frequencies
• PharmGKB — drug–gene interactions
• OMIM — Mendelian conditions
• Ensembl VEP — variant effect prediction

Medical advisors

Health content is reviewed by board-certified clinicians and genetic counselors before publication. Advisor names and credentials will be listed here at launch.

Privacy

HIPAA-aware architecture, GDPR-aligned data handling, encryption at rest and in transit, and an explicit consent model. Your DNA is never sold or shared without your written consent. You can export and delete your data at any time.