TraitDex
A complete index of your genome
Your DNA,in plain English.
Upload your raw 23andMe, AncestryDNA, or MyHeritage file. Every line in your report — ancestry, traits, drug response, disease risk — cites the study behind it. We pull from gnomAD, ClinVar, PharmGKB, PhyloTree, and the PGS Catalog: the same datasets used in published genetics research.
- Citations on every finding
- No accounts. No tracking.
Drop your raw DNA file
23andMe · AncestryDNA · MyHeritage · FamilyTreeDNA
.txt · .csv · .zip — up to ~25 MB
Match your paternal line to ancient skeletons.
Once we call your Y-haplogroup, we cross-reference it against 31,414 ancient-DNA samples sequenced from preserved bone and tooth in published archaeological studies. You may share an unbroken father-to-son line 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.
31,414 haplogroups indexed via the snipsa community curation. ~8 published ancient samples per call on average.
Every finding cites the study behind it.
Where your DNA points home
Continental ancestry across nine components — N. & S. Europe, Ashkenazi, Middle Eastern, W. African, E. & S. Asian, Dravidian, and Indigenous American. Built on the gnomAD HGDP+1KG reference panel (Koenig et al. 2024) — 4,094 published reference genomes. Bootstrap confidence intervals on every share. Optional FLARE haplotype-painting deep dive.
Maternal and paternal lines
mtDNA called against PhyloTree-17 via Haplogrep 3 — over 5,400 named maternal lineages spanning ~70,000 years of human migration. Y-DNA annotated against the YFull tree with time-to-most-recent-common-ancestor estimates.
Disease-risk patterns
Polygenic risk scores from the PGS Catalog (Lambert et al. 2021) and the APOE Alzheimer's diplotype from rs429358 + rs7412 (Corder et al. 1993). Each estimate flags ancestry applicability — most PGSes were trained on European samples. Not diagnostic.
How your genes shape medication response
1,385 genotype-specific rules across 128 PGx variants from CPIC and PharmGKB (Whirl-Carrillo et al. 2021) — the same evidence base used in clinical pharmacogenomics. Filtered to evidence levels 1A, 1B, and 2A.
Clinical variant cross-check
132,798 pathogenic and likely-pathogenic variants from the authoritative NCBI ClinVar VCF (Landrum et al. 2018). 1-star calls flagged with a chip-artifact warning — Weedon et al. 2021 measured a 96% false-positive rate for rare indels on consumer chips.
100+ everyday trait calls
Curated SNPs across pigmentation, taste, sleep, cognition, and athletic response — cross-referenced against SNPedia and ClinVar with composite combiners for eye color (HERC2 + OCA2, Sturm 2008), skin pigmentation, hair loss, and freckling.