Precision Genetics

Genetics, explained for the people who have to act on it.

Patient guides, clinic materials, and a family deck, written by a board-certified clinical molecular geneticist (DABMGG, FACMG). Every clinical statement carries its source.

Condition guide · first release

Coming soon

Lynch Syndrome: the patient guide

A plain-language book for people with Lynch syndrome and their families: what the result means, what to do next, what to ask, with the guideline or paper behind every statement printed inside. Paperback and Kindle on Amazon when released.

Amazon link when live

For clinics · non-geneticist practices

Coming soon

Lynch syndrome clinic license

$600 per clinic site, per year

For NPs, PAs, family practice, GI, oncology, and OB/GYN teams who see Lynch patients without a geneticist down the hall.

  • Patient side: the guide as a printable PDF plus handouts to print at the point of care
  • Clinician side: conversation scripts, patient FAQ, testing decision guide, referral guide, clinic workflow, insurance and legal notes, quick reference
  • Your practice name and phone on every handout · unlimited printing inside your site · education only, not a substitute for genetics referral
Buy when live

For families and classrooms

Coming soon

Genes We Share

$29.99 54-card deck

A kitchen-table genetics deck: how traits travel through a family, what "runs in the family" really means, and the questions worth asking your relatives. Non-clinical, light-hearted, no disease content.

Buy when live

Schools and homeschool co-ops

Classroom sets

Sets of 10 Genes We Share decks for a class, invoiced to a purchase order (W-9 on request), so a school can buy without a card. A free companion worksheet comes with each set.

To order: email hello@precisionhealthguides.com with your school name, number of sets, and billing contact.

About

Who writes this

A board-certified clinical molecular geneticist (DABMGG, FACMG) with a PhD in genetics and years of clinical laboratory directorship, writing for the patients, families, and clinicians who never get the geneticist in the room. Every clinical statement in every product is traced to a current guideline or peer-reviewed paper, cited where it appears.

Next conditions, as need shows: pharmacogenomics, Alzheimer's disease, familial hypercholesterolemia, universal genetic testing, hereditary breast cancer.

Education only. Nothing here is medical advice or a substitute for a genetics consultation; talk to your clinician or a genetics professional about your own situation.