What you can ask
The questions the experts argue about — answered from your own DNA.
The longevity and biohacker world is full of confident claims about genes, metabolizers, supplements and peptides. Indaga lets you check those claims against your own data — in plain language, with citations.
“Am I a slow caffeine metabolizer?”
Slow CYP1A2 keeps caffeine active hours longer — and changes when you should stop.
CYP1A2 · ADORA2AMetabolism“Do I have an MTHFR variant — should I take methylfolate?”
We show your genotype and what the evidence actually supports — not a supplement pitch.
MTHFR · COMT · VDRSupplements & peptides“What's my COMT status — warrior or worrier?”
How you clear dopamine under stress, with the honest size of the effect.
COMT Val158MetTraits & carrier“How do I metabolize this medication?”
Pharmacogenomics with calibrated guidance — and an honest note on what your chip could see.
CYP2D6 · CYP2C19 · CPICMedication“Is this peptide or supplement worth it for my genetics?”
Bring the compound the creators are talking about; get a cited, personalized read.
pathway-specificSupplements & peptides“What's my APOE genotype, and what does it actually mean?”
The most over-hyped variant in consumer genetics, explained without the scare.
APOE ε2/ε3/ε4Longevity“What does my DNA say about my lipid and metabolic biology?”
Polygenic context across many variants — calibrated to percentiles, never a verdict.
PGS · GWASLongevity“Am I a carrier for anything I'd want to know before kids?”
The standard carrier panel, screened locally, with callability stated honestly.
ACMG carrier — 113 genesTraits & carrier
Two directions, one engine
Start from a compound, or start from yourself.
Heard about a peptide or a supplement on a podcast? Ask what your genetics say about it. Curious how your own body handles caffeine, alcohol, or a medication? Ask that instead. Indaga resolves the genes involved, checks your genotype, and answers either way.
From a compound →
“Should I take creatine / NMN / this peptide for mygenetics?”
From yourself →
“What do I metabolize slowly, and how do I work with it?”
The honest part
Every answer says what it could — and couldn’t — see.
A consumer chip doesn’t read every position. When a variant isn’t callable from your file, Indaga tells you that plainly instead of pretending you’re in the clear. Absence is never “normal” — and a strong claim always comes with its evidence and its uncertainty.
Want answers from your own DNA?
Indaga is in active development. Join the waitlist and we’ll let you in as early access opens.