Due to system maintenance, the application system, application review by the Data Access Committee will be unavailable during the following period.
Schedule: October 5th (Mon), 2026, 9:00 - October 7th (Wed), 2026, 15:00 (JST)
We apologize for any inconvenience this may cause and appreciate your understanding.
We are currently receiving a large number of applications for data submission, and the review process is taking longer than usual.We sincerely apologize for the delay and kindly ask for your understanding. When submitting an application, we would greatly appreciate it if you could allow sufficient time for the processing.
Following a change to our organizational structure effective April 1, 2026, this division has been renamed from the "Database Center for Life Science, Joint Support-Center for Data Science Research" to the "Database Division for Life Science (DBCLS), BioData Science Initiative (BSI), National Institute of Genetics (NIG)". Where the former name still appears in the guidelines, please read it as the new name.
Dataset ID
NHA000203
Type of data
Genome-wide gene-environment interaction studies for clinical traits and metabolites (374 phenotypes)
HumanExome BeadChip Kit HumanOmniExpress BeadChip Kit HumanOmniExpressExome BeadChip Kit UK BiLEVE Axiom Array UK Biobank Axiom Array
Platform
Applied Biosystems UK BiLEVE Axiom Array Applied Biosystems UK Biobank Axiom Array Illumina HumanExome Illumina HumanOmniExpress Illumina HumanOmniExpressExome
QC and filtering
Clinical Phenotypes: imputation quality > 0.7, minor allele frequency (MAF) > 0.01, autosomal variants Metabolome: further restricted to (i) genotyped variants, (ii) HapMap3 variants, and (iii) the variants with P_G×E < 1.0×10^-7 in BBJ or UKBB for at least one of the clinical traits