Evidence-scoped
Each result answers only the question supported by the input and reference evidence.
Interpret a DNA match total or explore established genetic traits from a commercial raw DNA export. Every tool shows its evidence and where the answer stops.
Start with the total reported by your testing service. No DNA upload or account is required.
Each calculator processes the uploaded file only for the request and returns partial or unavailable coverage honestly.
Common A, B, AB, or O inference from a three-marker haplotype panel.
Open calculator →Read the six established eye-colour markers used by the IrisPlex panel, with a conservative result that keeps intermediate colours and missing data visible.
Open calculator →Check the common Eurasian lactase-persistence enhancer plus functional variants documented in African and West Asian populations.
Open calculator →Interpret CYP1A2 rs762551 enzyme inducibility and, when available, keep the separate ADORA2A caffeine-response marker in context.
Open calculator →Resolve the common TAS2R38 PAV and AVI haplotypes that shape sensitivity to the laboratory bitter compounds PTC and PROP.
Open calculator →Read the strongly predictive ABCC11 rs17822931 variant associated with wet or dry earwax, with strand orientation made explicit.
Open calculator →Preview marker overlap from a supported raw DNA export, then unlock Transformer-assisted reference inference.
Open module →Each result answers only the question supported by the input and reference evidence.
A missing marker is reported as missing—never interpreted as the reference genotype.
Sources, ranges, marker calls, model roles, and important limitations stay visible.
Continue with a free global ancestry preview, then unlock the detailed full report with regional components and closest-population comparisons.