dna-seq on GitHubJust-DNATry the demo

What a report holds

Findings

The Longevity Variants report: totals of matched variants, then a table with genotype, zygosity and weight, and one FOXO3 finding opened to its conclusion and direction.
Evidence you can follow
rsIDs link to dbSNP, studies to PubMed.
Results in a sentence
Blood group or APOE type as one plain answer.
Gaps are labelled
Inferred genotypes and skipped modules say so.

Polygenic scores

Every score model, side by side

Different studies built different models for one trait, and they often disagree. just-prs scores your genome with each PGS Catalog model.

Most models come from studies of European ancestry.

A polygenic score report for LDL cholesterol: summary tiles above a bell curve with each model’s position marked.
101 LDL cholesterol models for one public genome.

How to read it

Before you read a result as news

Understanding your genome

Not a diagnosis
Health decisions belong with a clinician or a genetic counsellor.
Red labels are common
Healthy genomes carry variants once called pathogenic.
A score is a place on a chart
Lifestyle often matters more than any common variant.
Worried? Ask a doctor
A finding that matches your family history needs a clinical test.