One cheek swab, four areas of insight, over 400 reports — for medical professionals, researchers and institutional clients.
Quantified risk across multifactorial conditions where the genetic contribution is well characterised. Reported as risk relative to a reference population, with the contributing variants listed so the result can be interrogated rather than merely read.
Monogenic conditions across recessive and dominant inheritance patterns. Carrier findings are reported as carrier status without implication of phenotype — relevant to reproductive counselling and to family-history work.
Metabolism and response profiles across commonly prescribed classes, reported against established guideline categories so findings map onto prescribing frameworks clinicians already use.
Pharmacogenomic results inform prescribing decisions; they do not replace them. No patient should start, stop, or alter the dose of any medication on the basis of this report without consulting their prescribing physician.
Nutrient and micronutrient metabolism, caffeine and alcohol processing, physical and sensory traits, and biogeographical ancestry with maternal and paternal lineage assignment.