Tendencies, not verdicts
A genetic variant nudges a probability; it doesn't write your future. I refuse to use scary language about risk, because the honest story is almost always "here's a lever you can pull," not "here's your fate."
Gene Compass didn't start as a project. It started as one unread file sitting in a downloads folder — and one rainy weekend with too much coffee and too many questions.
Like a lot of people, I took a DNA test expecting an ancestry pie chart. I got the pie chart. But buried in the account settings was a button most people never press: “Download raw data.”
That button hands you a text file with hundreds of thousands of rows — each one a tiny spelling difference in your DNA, called a SNP ("snip"). On its own the file is unreadable, like being given a phone book in a language you don't speak. But every one of those rows has been studied somewhere: in papers about caffeine, sleep, vitamin D, muscle fibers, stress chemistry, how you metabolize medicine.
So I started looking things up. One marker became ten. Ten became an evening. An evening became a spreadsheet, the spreadsheet became a folder of research notes, and the folder eventually became something with a name on the door: Gene Compass — ten plain-English reports and a living dashboard, built by hand from a person's own raw data.
I'm not a geneticist and I don't pretend to be one. I'm a careful amateur with a good filing system, a respect for peer-reviewed sources, and a rule that I never overstate what a marker means. The honest framing is the one I named the project after: your genes are a compass. They point at tendencies. They don't decide where you go.
I downloaded my raw DNA data on a whim and discovered 640,000+ markers nobody ever looks at. The ancestry chart took five minutes; this file has taken years — happily.
Nights and weekends spent learning the vocabulary: genotypes, effect alleles, methylation, pharmacogenomics. I leaned on peer-reviewed literature and learned to be suspicious of any source that promised too much.
I wrote a complete ten-report set for a family member — diet, disease prevention, metabolism, exercise, detox, brain chemistry, gut health, drug metabolism, hormones, and a final report tying it all together. Every line auditable back to the raw file.
Hundreds of pages are wonderful and useless at 7 a.m. So everything got distilled into one living dashboard and a ten-item daily protocol — the difference between a library and a guide.
This site. A home for the hobby, a way to show friends and family what's possible with a file they already own — and maybe, someday, the seed of something bigger.
A genetic variant nudges a probability; it doesn't write your future. I refuse to use scary language about risk, because the honest story is almost always "here's a lever you can pull," not "here's your fate."
Each genotype in a report lists the exact marker it came from, so anyone — including a physician — can check my work against the raw file. If a marker wasn't in the data, I say so instead of guessing.
Genetic data is the most personal file a person can own. Everything I analyze stays private, the samples on this site use an invented demo profile, and nothing real is ever published or shared.
The full process — from raw file to finished compass — explained for non-scientists, with honest notes about what this can and can't tell you.