Skip to content
NBDC Human Database

No datasets in the cart.

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

NHA000075

Type of data
meta analysis of 2 GWASs for T2DM with diabetic nephropathy
Access criteria
Unrestricted-access
Total data volume
318 MB
File formats
  • XLSX
  • ZIP
Research
hum0014
Date published
2018-12-10
Date modified
2018-12-10
Secondary ID
hum0014.v12.T2DMwN.v1, hum0014.v12.T2DMw.v1

Unrestricted-access files linked to this dataset

FileLabelSizeCopy URL
header_definition_hum0014.v12.xlsxDictionary file11.5 KB
hum0014.v12.T2DMwN.v1.zip318 MB

Analysis method

Genotyping by array

Materials and participants
[GWAS-1]
- 2,380 T2DM with diabetic nephropathy patients
- 5,234 T2DM without diabetic nephropathy patients
[GWAS-2]
- 429 T2DM with diabetic nephropathy patients
- 358 T2DM without diabetic nephropathy patients
  • Health status
    Affected
  • Subject count
    8401 (Individual)
Sample description
gDNA extracted from peripheral blood cells
  • Tissue
    Peripheral blood
  • Tumor / normal
    Normal
Sample provider
N/A
Experimental method
Genotyping by array
Target
N/A
Reagent kit
Human610-Quad BeadChip Kit
HumanOmniExpressExome BeadChip Kit
Platform
Illumina Human610-Quad
Illumina HumanOmniExpressExome
Reference genome
GRCh37
QC and filtering
sample call rate < 0.98, SNV call rate < 0.99, MAF < 0.1%,
HWE P < 1 x 10⁻⁶ in control
Imputation
MACH and Minimac (1000 Genomes phased JPT, CHB and Han Chinese South data n = 275, March 2012)
Analysis method
GenCall software (GenomeStudio)
Variant count
7,521,072 SNPs