Pocket Genes

A genomic companion for navigating uncertainty.

Pocket Genes helps people and families bring scattered genetic information together, understand complex concepts, prepare better medical conversations, and find support when the path is rare, long, or confusing.

The positioning shift

Not just a report viewer. A way to turn genetic data into useful context.

Pocket Genes is designed to organize reports, panels, providers, test history, inheritance concepts, and possible next questions in one clear place. The goal is not to replace physicians or genetic counselors, but to help people arrive better prepared.

1place for reports, panels, and PDFs
0diagnoses or clinical instructions inside the app
24/7organized information before an appointment

What Pocket Genes needs to solve

The experience is organized around real needs families face when genetic questions are difficult.

Organize information

Bring reports, files, panels, labs, dates, analyzed genes, and family notes together so important context is not lost.

Understand concepts

Explain variants, inheritance, carrier status, penetrance, panels, sequencing, and pharmacogenomics in accessible language.

Prepare conversations

Help identify what was analyzed, what may be missing, and which questions to bring to a physician or genetic counselor.

Find support

Connect people with associations, resources, registries, specialists, and others navigating similar questions.

For families

From loose files to an organized genetic story

Many families arrive at genetics after years of symptoms, referrals, tests, and PDFs that are hard to compare. Pocket Genes turns that accumulation into a timeline people can actually use.

Test history

Save which test was done, when, with which provider, and what type of panel or technology was used.

Genetic coverage

Separate analyzed genes, genes not covered, and areas where another test or specialist discussion may be needed.

Appointment notes

Turn scattered concerns into clear questions for the medical team.

Organized genomic report interface

For the ecosystem

A bridge between patients, providers, and community

The same base that lets providers integrate reports can also help families compare coverage, understand results, organize resources, and reach support networks.

Comparable providers

Understand which panel, lab, or service covers which genes, conditions, or needs.

Trusted resources

Surface associations, registries, educational guides, and relevant specialists based on context.

Privacy first

Give people control over what information is stored, shared, and with whom.

Phone beside a lab pipette

Clear clinical boundaries

Pocket Genes does not diagnose, prescribe, or replace health professionals. Its role is to help people organize information, understand concepts, and prepare better conversations.

  • Educational language, not medical instructions.
  • Separates reported findings from questions that need professional interpretation.
  • Encourages consultation with physicians, geneticists, and genetic counselors.

Two narratives, one platform

Families need clarity and support. Providers need a serious way to deliver mobile reports. Pocket Genes connects those needs without mixing them.