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-NPU-MDS, TBD, HMB-MDS, NA, DS-EPI-ASZ-MED-MDS, GRU, DS-ASD, DS-CVD-IRB-COL-MDS, DS-LMC-IRB, HMB, DS-DRC-IRB-NPU, GRU-IRB-COL, EPIL_BRAIN_AB_INTEL_DIS_MDS, DS-IBD, EPIL_CO_MORBIDI_MDS, 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-CARDI_NEURO, DS-AONDD-IRB, HMB-IRB-MDS, HMB-NPU, HMB-IRB-PUB, DS-ASD-MDS-PUB, DS-LD-RD, Unspecified, DS-IRB-MDS, DS-CVD, DS-EAED-MDS, DS-GID, DS-NEURO-MDS, HMB-IRB, DS-NPD-IRB-NPU, HMB-GSO, DS-EP, DS-NEURO-AD-NPU, DS-EPI-MUL-CON-MDS, DS, HMB-IRB-PUB-COL, DS-MH, DS-GI,18+, DS-ATHSCL-IRB-MDS, DS-ASD-MDS, HMB_MDS, EPIL_BRAINAB_CONVUL_INTELCT_DIS_MDS, EPIL_BRAIN_AB_MDS, DS_GI_18+_MDS, HMB-NPU-ADULTS, DS-EP-MDS, DS-IBD-MDS, DS_IBD_MDS, GRU-MDS-PUB, DS-SEIZD, HMB-PUB, DS-EPI-COMO-MDS, DS-ND, DS-CAD-PUB-MDS, DS-EAC-PUB-GSO, DS-EP-NEURO-MDS, DS-EPIL-BC-ID-MDS, DS-EP-ETIOLOGY-MDS, 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, NA, Autism Spectrum Disorder, --

Study Design

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

Data Types

Exome, Genotyping Array, Whole Genome, Unspecified, TBD

Subjects

436,761