The database of Genotypes and Phenotypes (dbGaP) was developed to archive and distribute the results of studies that have investigated the interaction of genotype and phenotype.

Latest Studies

Important notice: NIH has established a collection of dbGaP samples designated as appropriate for general research use (GRU) by submitting institutions, which indicates that there are no further limitations on secondary research use beyond those outlined in the Genomic Data User Code of Conduct. For details, visit the collection's page.
Study Embargo Release Details Participants Type Of Study Links Platform
Comparison of custom capture for targeted next generation DNA sequencing

Version 1:
V D A S 10 Mixed, Cross-Sectional, Tumor vs. Matched-Normal
Autosomal recessive TPP2 mutations cause a new human immunodeficiency

Version 1: 2015-12-16
V D A S 3 Case-Control Links
Genome Analyzer IIX
Whole Genome Sequencing of HUES63 and HUES64
Version 1: passed embargo
V D A S 2 Control Set Links
HiSeq 2000
HiSeq 2500
DNA Methylation age and mortality in the Lothian Birth Cohorts

Version 1: 2015-11-12
V D A S 1366 Longitudinal Cohort Links
450K Infinium Methylation
Autosomal recessive PGM3 mutations cause a new Congenital Disorder of Glycosylation
Version 1: passed embargo
V D A S 8 Parent-Offspring Trios Links
HiSeq 2000
List Top Level Studies
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