Coverage-aware
A missing marker is reported as missing—never interpreted as the reference genotype.
Six focused calculators for established genetic traits. Upload an unmodified commercial DNA export, inspect every marker used, and see exactly where the evidence stops.
Every calculator is free, processes the 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 →A missing marker is reported as missing—never interpreted as the reference genotype.
Each result describes the phenotype actually studied, with population and environmental limits visible.
The rsIDs, raw calls, model role, research references, and version are all exposed.
Continue with a free global ancestry preview, then unlock the detailed full report with regional components and closest-population comparisons.