rs10757278
W:2.40
49%
9p21 risk locus (G/G) - the most replicated common variant for coronary artery disease.
Genetic research engine
A 25,000+ page deep-research report on your own DNA - your genome read against 4,000+ topics (diseases/traits) and the scientific literature, analysed by frontier models over 1.5 trillion tokens of recent papers. Search it like documentation. Summarized, ranked for relevance and grouped by topics with polygenic scores.
Zero data retention
coronary artery disease
Your score vs population
lower riskhigher risk
How it reads your genome
From raw alleles to a report you can actually use.
-
01
Upload. Drop in your provider's raw file. We compute an anonymous genome hash, never store the file, and process it in memory.
-
02
Match. Your genotypes are mapped to 100k+ curated SNPs, variant groups and 4,000+ topics, each scored against the general population.
-
03
Read. Search diseases, drugs, genes and rs-IDs. Every finding carries a plain-language take and links to dbSNP, the GWAS Catalog and the papers behind it.