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Study Description

We report a genome-wide association study of IgA nephropathy, a main cause of kidney failure. All subjects were of Chinese Han ancestry, of which 1,194 were cases and 902 controls. Genomic DNA samples extracted from whole blood were genotyped on the Illumina 610 Quad platform.

  • Study Type: Case-Control
  • Number of study subjects that have individual level data available through Authorized Access: 2096

Authorized Access
Publicly Available Data (Public ftp)

Connect to the public download site. The site contains release notes and manifests. If available, the site also contains data dictionaries, variable summaries, documents, and truncated analyses.

Study Inclusion/Exclusion Criteria

The inclusion criterion for cases was confirmation of affected status by renal biopsy. Control participants were healthy blood donors.

Molecular Data
TypeSourcePlatformNumber of Oligos/SNPsSNP Batch IdComment
Whole Genome Genotyping Illumina Human610_Quadv1_B 601273 1048904
Selected publications
Diseases/Traits Related to Study (MESH terms)
  • Primary Phenotype: Glomerulonephritis, IGA
Authorized Data Access Requests
Study Attribution