Genomics Hub

Open genomic intelligence — search variants, explore drug-gene interactions, map disease genetics, and browse signalling pathways. All data is free and open. Contribute anonymised genomic data to accelerate research for neglected diseases.

Sources: ClinVar, OMIM, PharmGKB, KEGG, UniProt, GWAS Catalog

Variant Search

Search any gene or variant by name or rsID. Clinical significance, population frequency, and drug interactions.

Disease Genetics

Genetic architecture of diseases — risk genes, heritability estimates, protective variants, and GWAS associations.

Pharmacogenomics

Drug-gene interaction database. Enter a drug and variant to see predicted response and dosing guidance.

Pathway Explorer

Major signalling pathways — mTOR, PI3K-Akt, MAPK, NF-kB — the genes involved and drugs that target them.

Open Sequences

Genomic datasets donated to humanity. Browse and contribute anonymised sequences — no restrictions, free forever.

Privacy

How we protect genomic data. Differential privacy, aggregation, GDPR compliance, and your right to deletion.