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Upload a consumer genotype export or a single-sample VCF to keep variant calls in the selected person’s record. Genetic test reports remain ordinary documents; raw genotype files use a separate import and query workflow.

Supported uploads

The importer recognizes supported text and CSV exports, including 23andMe, AncestryDNA, MyHeritage, FTDNA and WeGene, plus VCF and supported compressed containers. A ZIP with multiple genotype files and a multi-sample VCF are rejected because the intended file or sample is ambiguous. The Data page shows import status. A successful import activates the new set; re-uploading replaces the active collection. A failed import leaves the previous active set available.

Queries

Region queries use GRCh37, GRCh38 or explicitly raw coordinates. Results retain call status and source information. An unsupported or ambiguous call stays unresolved; an absent site or no_call is not a normal result. Pharmacogenomic coverage does not establish a phenotype or prescribing advice. The current tool returns not_determined for phenotype rather than inferring star alleles from incomplete array data. Rare variant calls are not converted into disease diagnoses.

Export

The active collection can be exported as VCF, or selected rsIDs as FHIR variant observations. Use your own account token; see data export. Build handling, supported layouts and query examples are in the genetics reference.