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, TBD, HMB-MDS, DS-MBND-NPU-MDS, DS-NSD-NPU-MDS, DS-EPASM-MDS, GRU, DS-ASD, DS-CVD-IRB-COL-MDS, DS-LMC-IRB, HMB, DS-DRC-IRB-NPU, GRU-IRB-COL, DS-EPSBAID-MDS-RD, DS-IBD, DS-EPCOM-MDS-RD, HMB-NPU-MDS, Consortia Access Only, DS-EP-NPU, DS-GI, DS_GI, DS-CVDRF, DS_GI_IRB_MDS, GRU-IRB, DS-CARD-MDS-GSO, GRU-IRB-NPU, DS-ASD-IRB, DS-CARNEU-MDS, DS-AONDD-IRB, HMB-IRB-MDS, HMB-NPU, HMB-IRB-PUB, DS-ASD-MDS-PUB, DS-LD-RD, Unspecified, DS-IRB-MDS, DS-CVD, NA, DS-EAED-MDS, DS-GID, DS-NEUROLOGY-MDS, HMB-IRB, DS-EP-MDS, DS-NPD-IRB-NPU, HMB-GSO, DS-NEUROLOGY-ADULTS-NPU, DS-EPI-MULTI-MDS, DS, DS-EP, HMB-IRB-PUB-COL, 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, GRU-MDS-PUB, DS-SEIZD, HMB-PUB, DS-ND, DS-CAD-PUB-MDS, DS-EAC-PUB-GSO, DS-EAED-IRB-NPU-MDS, DS-EPSBACID-NPU-MDS-RD, DS-EPASM-MDS-RD, DS-CVD-IRB, DS-EARET-MDS, DS-CAD-IRB-COL-NPU, GRU-IRB-PUB, GRU-GSRS, DS-ASD-IRB-PUB-COL-NPO-GSO, HMB_IRB_MDS

Diseases

inflammatory bowel disease, epilepsy, Epilepsy, coronary artery disease, autism spectrum disorder, cardiovascular system disease, type 1 diabetes mellitus, atrial fibrillation, cardiovascular disease and risk factors, atherosclerosis, hemorrhagic stroke, Alzheimer's disease, cardiovascular disease, asthma, Unspecified, myocardial infarction, heart and blood vessel disease, N/A, control, Autism Spectrum Disorder, --, Control

Study Design

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

Data Types

Exome, Genotyping Array, Whole Genome, Unspecified, TBD

Subjects

436,761