TraitDex

A complete index of your genome

Open methodology

Your genome,indexed as a complete catalog.

Upload your raw 23andMe, AncestryDNA, or MyHeritage file. TraitDex maps it against published reference panels — gnomAD, PhyloTree, ClinVar, PharmGKB, the PGS Catalog — and renders the result as an explorable report.

  • Derived from published datasets
  • No accounts. No tracking.

Drop your raw DNA file

23andMe · AncestryDNA · MyHeritage · FamilyTreeDNA

.txt · .csv · .zip — up to ~25 MB

No accounts · No tracking
132,798
ClinVar variants checked
31,400
Ancient DNA matches
1,385
Drug-response rules
5,400+
Maternal lineages
Ancient DNA

Find your deep cousins on archaeological skeletons.

Once we call your Y-haplogroup, TraitDex matches it against thousands of ancient-DNA samples sequenced from preserved bone and tooth in published studies. You may share an unbroken father-to-son chain with a Bronze Age chieftain, a Viking warrior, an Iberian Muslim burial, or a Neolithic farmer — sometimes by a few centuries, sometimes by tens of thousands of years.

Sourced from the snipsa Y-haplogroup database. 31,400 haplogroups indexed, 8 ancient samples per call on average.

R-M2691100–1300 CE
Iberian Muslim burial
Andalusia
I-M253800–1100 CE
Viking warrior
Denmark
R-P3121800 BCE
Bronze Age horseman
France
G-P156000 BCE
Neolithic farmer
Anatolia
What you'll see

Six layers, one structured index

Where your DNA points home

Nine-component continental mixture with bootstrap intervals — N. & S. Europe, Ashkenazi, Middle Eastern, West African, East & South Asian, Dravidian, and Indigenous American. Optional FLARE haplotype-painting deep dive.

Maternal and paternal lines

mtDNA called against PhyloTree-17 via Haplogrep 3 — over 5,400 named clades. Y-DNA annotated with TMRCA estimates from YFull.

Polygenic risk & APOE

Population-level risk scores from the PGS Catalog plus APOE Alzheimer's diplotype. Every estimate is paired with an ancestry applicability indicator. Not diagnostic.

Drug-response patterns

CPIC and PharmGKB clinical annotations — over 1,300 curated rules across 128 PGx variants. Findings ranked by actionability and evidence level (1A / 1B / 2A).

ClinVar cross-check

Pathogenic and likely-pathogenic variants from the authoritative NCBI ClinVar VCF — searchable, filterable, with chip-artifact warnings on 1-star calls (Weedon 2021).

100+ trait calls

Curated SNPs across pigmentation, taste, sleep, athletic, and cognitive categories — cross-referenced against SNPedia and ClinVar with composite-trait combiners (eye color, skin pigmentation, hair loss, freckles).