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Atlas
Genómico
Fictitious patient data · Not a medical result
Genomic report

Martín Fernando Gómez

42 years old · Male

Protocol
DEMO-2026-000123
Sample
14/07/2026
Issued
05/08/2026

You are seeing only the results that can change clinical managementYou are also seeing the results that change no clinical management

Levels C and D are replicated, but there is no evidence that knowing them improves an outcome: that is why the report does not open with them.

Summary

What this test found, on one screen. Every number leads to the detail, and the detail always says how much was measured to get there.

From your genome to what was read
Your genome
3.2 billion

letters. One in every 4,893 is measured.

What the chip measures
654,027

selected positions: the ones that vary between people and the ones evidence links to something.

99.4%
What was read in your sample
650,103

of the 654,027 the chip measures returned a genotype.

The three panels are not to scale with each other: the drop from the genome to the chip spans four orders of magnitude and drawing it would reduce the last two to nothing. The only percentage in the figure is in the third one, where both quantities share the same unit.

Ancestry composition
See the map →
European71.4%Indigenous American22.8%Sub-Saharan African4.1%South Asian0.9%Unassigned0.8%
Maternal lineage
D1
Paternal lineage
R1b-M269

A single unmixed line of the family: the maternal one comes from mother to mother to mother, and the paternal from father to father. That is why they are two codes and not a percentage.

The 29 drugs, by band
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Significant interaction2Moderate interaction10No result5Use as directed12

Sections

How to read everything that follows

No section of this report gives a diagnosis. Every result comes with how much was measured to reach it, because a “nothing was found” is worth exactly what the coverage of that gene is worth. There are 11 sections and they can be read in any order.