AnVIL Dataset Catalog

CCDG

The Centers for Common Disease Genomics are a collaborative large-scale genome sequencing effort to comprehensively identify rare risk and protective variants contributing to multiple common disease phenotypes.

Consent Codes

DS_IBD, GRU-NPU, DS-EPI-ADULT-NPU-MDS, HMB-MDS, DS-MBND-NPU-MDS, DS-NSD-NPU-MDS, DS-EPASM-MDS, DS-ASD, DS-CVD-IRB-COL-MDS, HMB, DS-DRC-IRB-NPU, GRU, DS-EPSBAID-MDS-RD, DS-IBD, DS-EPCOM-MDS-RD, HMB-NPU-MDS, DS-EP-NPU, DS-GI, DS_GI, DS_GI_IRB_MDS, GRU-IRB, DS-CARD-MDS-GSO, TBD, DS-ASD-IRB, DS-CARNEU-MDS, DS-AONDD-IRB, HMB-IRB-MDS, DS-ASD-MDS-PUB, Unspecified, DS-EAED-MDS, DS-GID, DS-CVD, DS-NEUROLOGY-MDS, HMB-IRB, DS-EP-MDS, HMB-NPU, DS-NPD-IRB-NPU, DS-NEUROLOGY-ADULTS-NPU, Consortia Access Only, DS-EPI-MULTI-MDS, DS, DS-EP, DS-MH, DS-GI,18+, DS-ATHSCL-IRB-MDS, DS-ASD-MDS, HMB_MDS, DS-EPSBACID-MDS-RD, DS-EPSBA-MDS-RD, DS_GI_18+_MDS, HMB-NPU-ADULTS, DS-NSD-ADULTS-NPU-MDS, DS-NEURO-EP-MDS, DS-IBD-MDS, DS_IBD_MDS, NA, GRU-MDS-PUB, DS-SEIZD, DS-ND, DS-EAC-PUB-GSO, DS-EAED-IRB-NPU-MDS, DS-EPSBACID-NPU-MDS-RD, DS-EPASM-MDS-RD, DS-EARET-MDS, DS-CAD-IRB-COL-NPU, GRU-GSRS, HMB-GSO, HMB_IRB_MDS

Diseases

inflammatory bowel disease, epilepsy, Epilepsy, autism spectrum disorder, cardiovascular system disease, type 1 diabetes mellitus, atherosclerosis, hemorrhagic stroke, Unspecified, control, myocardial infarction, coronary artery disease, atrial fibrillation, --, Control

Study Design

Case-Control, Case Set, Case set, Family/Twins/Trios, TBD, Family, Parent-Offspring, Unspecified, Control Set, Parent-Offspring Trios, Parent-Offspring Quads, Clinical Trial, Case-control, Prospective Longitudinal Cohort, Control

Data Types

Exome, Whole Genome, Genotyping Array, Unspecified, TBD

Subjects

267,862