---
title: Searching the full report
description: How to search all your variants, use the suggestions and filters, and search inside a category.
date: 2026-10-07
category: Guide
image: img/blog/search_cover.png
image_alt: The full report searched for lactose, with the Frequency and Risk filters and the card for rs4988235
---

The full report is every variant in your report with a summary, in one list you can search. Open it with "Full report" in the top menu. With nothing typed, it shows all your variants, the highest-impact ones first.

## Searching

Type a condition, a trait, a drug, a gene or an rsID in the search box, then press Enter.

![The full report searched for lactose, showing the card for rs4988235(C;C)](static:img/blog/search_results.png)

Each result is a variant card, and more load as you scroll. [Variant geno card explained](/blog/geno_card) walks through everything on a card. You'll also see a few variant groups: sets of variants that are read together, like a haplotype. The [FAQ](#faq:variant_groups) explains them.

If you type an rsID, such as rs4988235, the search goes straight to that variant when it's in your report.

On the free tier you can search everything and read each variant's short summary. The full analysis opens on a few cards, marked as free to read, and on all of them once you unlock all your reports.

## Suggestions as you type

After a few letters, a list of suggestions opens under the search box.

![Suggestions for omega: three search terms, then three reports under Reports](static:img/blog/search_autocomplete.png)

The top part is search terms: pick one to search for it. Under "Reports" are the matching reports, each with a `GWAS` badge. Pick one of those to go straight to the report page. [Understanding your reports](/blog/reports) explains what you'll find there.

## Filters

Two filters sit at the right of the search box. They work with or without a search.

**Frequency** narrows the list by how common your exact genotype is in the population:

![The Frequency menu: Any frequency, Common under 50%, Infrequent under 10%, Rare under 5% and Very rare under 1%](static:img/blog/search_frequency.png)

**Risk** narrows it by the colored dot next to the impact score:

![The Risk menu: Any risk, Good, Warning, Bad and Info](static:img/blog/search_risk.png)

- **Good:** protective or beneficial genotypes.
- **Warning:** an impact score between 2 and 3.
- **Bad:** an impact score above 3.
- **Info:** neutral, informational findings.

When a filter is on, its button shows your choice, for example "Infrequent (<10%)" or "Warning". The × at the end of the search box clears the search and both filters.

Combining them is often the quickest way in. Rare and Bad together, for example, show your uncommon genotypes with the strongest impact. Rare doesn't mean harmful, though, so read the summary before drawing conclusions.

## Searching inside a category

The left menu lists 15 categories, from Aging to Vision. On a phone, open it with the menu button at the top left.

![The Categories list in the left menu, with Metabolic selected](static:img/blog/search_categories.png)

Picking a category opens the full report showing only the variants in that category, with the ones that weigh most in it first. The search box stays at the top, with a "Category" chip in it, so you can search inside the category and use the filters there too.

![The search box with the Category: Metabolic chip, searched for caffeine](static:img/blog/search_category.png)

Here the Metabolic category is searched for caffeine. Click the × on the chip to go back to searching your whole report.

## Where else to look

- The **Rare variants** page, in the left menu, lists only your uncommon genotypes: those fewer than 5% of people carry, a cutoff you can change on the page.
- **Favorites** collects the cards you've starred, so you can come back to them. With all your reports unlocked, "Save as PDF" on that page saves them to a PDF.