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Transparency · Real content

Sample reports

Download real anonymised reports and check for yourself the level of detail, clarity and clinical utility before ordering any test.

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Total transparency

See before you order

We are the only Spanish genomics laboratory that publishes its real reports (anonymised) openly. Because you cannot make an informed decision if you don’t know what you will receive.

Cardiology panel (SCD)

Study of cardiomyopathies, channelopathies and aortopathies in a patient with family sudden cardiac death. 174 genes, ACMG variants and complete clinical report.

PDF · 38 pages

Cancer predisposition

Hereditary oncology panel in a patient with family history of breast and ovarian cancer. Pathogenic variant in BRCA1, family risk and recommendations.

PDF · 42 pages

Complete personal genome

Real consumer report example: ancestry, 130+ traits, PRS, nutrigenetics, pharmacogenomics and clinical variants. Generated from GenePortal.

PDF · 86 pages

Fertility · Couple screening

Carrier screening test in a couple planning pregnancy. 300+ recessive diseases, cross analysis and transmission risk calculation.

PDF · 28 pages

Paediatric exome

Clinical trio exome (girl + parents) in a case of developmental delay and dysmorphic traits. De novo pathogenic variant and molecular diagnosis.

PDF · 34 pages

Pharmacogenomics

Complete PGx report with response to 120+ medications, CYP, DPYD, TPMT, SLCO1B1 haplotypes and recommendations according to CPIC and FDA guidelines.

PDF · 52 pages
Important note

They are real reports, not mock-ups

All PDFs available on this page are real reports issued by OmicaLabs to patients or professionals, duly anonymised. Names, ID numbers, exact dates and any direct identifiers have been removed, in accordance with AEPD and ICO anonymisation guidelines.

The scientific content, structure, interpretation and recommendations are exactly what you will receive if you order the same type of study.

What you will find in each report

Common structure

  • Executive summaryA single page with the key findings and main recommendations, ready to share with your physician.
  • Clinical contextDescription of the study reason, methodology used and known limitations.
  • Identified variantsComplete listing with ACMG/AMP classification, applied criteria, population frequencies and references.
  • InterpretationClinical significance of each finding, follow-up recommendations and family counselling.
  • Technical appendicesCoverage, quality metrics, full list of analysed genes and bioinformatics pipeline.
  • Clinical sign-offReport signed by a registered specialist geneticist, with date and registration number.

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