For research & industry
Saudi-specific
genomic insights
for medical R&D.
Request access to aggregated, de-identified data on the most common genes, variants, and carrier frequencies observed across the Kingdom — curated by the Saudi Genome clinical and laboratory network.
120K+
Profiles in scope
13
Saudi regions covered
100%
De-identified
genome.sa / dataset / preview.json
{
"gene": "HBB",
"variant":"NM_000518.5:c.20A>T",
"region": "Eastern Province",
"carrier_freq": 0.041,
"sample_n": 8421,
"consanguinity_flag": true,
"release": "v2026.Q2"
}What's available
Datasets curated for Saudi-focused research
All releases are aggregated and de-identified. Cell-level suppression and regional binning are applied automatically to prevent re-identification.
Common-variant atlas
Allele and carrier frequencies for clinically actionable genes across the Saudi population.
Regional breakdowns
Province- and region-level variant prevalence with consanguinity stratification.
Pharmacogenomics
Frequencies of CYP, DPYD, TPMT and other PGx variants relevant to Saudi prescribing.
Carrier screening
Premarital and family-screening cohorts for autosomal recessive disorders.
Custom cohorts
Define a phenotype, gene panel, or regional slice and request a tailored extract.
Governed access
Data Use Agreement, IRB review, and access tier reviewed by our scientific board.
Process
From request to data delivery
- 1
Submit
Tell us about your organization, intended use, and the dataset you need.
- 2
Review
Our scientific committee reviews scope, ethics, and feasibility within 10 working days.
- 3
Agreement
Sign a Data Use Agreement and provide IRB / ethics approval.
- 4
Access
Receive a secure download link or API credentials for your release.
Application
Request data access
All fields marked * are required. We'll reply within 10 working days.