dbGaPapplication/xmlftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/release_notes/Release_Notes.phs001502.CCDG_UPenn_EOCAD.v1.p1.MULTI.pdfftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/manifest/Study_Report.phs001502.CCDG_UPenn_EOCAD.v1.p1.MULTI.pdfftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/manifest/manifest_phs001502.CCDG_UPenn_EOCAD.v1.p1.c1.HMB-IRB-PUB.pdfftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/pheno_variable_summaries/phs001502.v1.pht007259.v1.CCDG_UPenn_EOCAD_Sample.data_dict.xmlftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/pheno_variable_summaries/phs001502.v1.pht007258.v1.p1.CCDG_UPenn_EOCAD_Subject.var_report.xmlftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/pheno_variable_summaries/phs001502.v1.pht007260.v1.p1.CCDG_UPenn_EOCAD_Subject_Phenotypes.var_report.xmlftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/pheno_variable_summaries/phs001502.v1.pht007261.v1.p1.CCDG_UPenn_EOCAD_Sample_Attributes.var_report.xmlftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/pheno_variable_summaries/phs001502.v1.pht007261.v1.CCDG_UPenn_EOCAD_Sample_Attributes.data_dict.xmlftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/GapExchange_phs001502.v1.p1.xmlftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/pheno_variable_summaries/phs001502.v1.pht007258.v1.CCDG_UPenn_EOCAD_Subject.data_dict.xmlftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/pheno_variable_summaries/phs001502.v1.pht007260.v1.CCDG_UPenn_EOCAD_Subject_Phenotypes.data_dict.xmlftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/pheno_variable_summaries/phs001502.v1.pht007259.v1.p1.CCDG_UPenn_EOCAD_Sample.var_report.xmlftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/pheno_variable_summaries/varreports_v3.xslftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/pheno_variable_summaries/datadict_v2.xslftp://ftp.ncbi.nlm.nih.gov/dbgap/studies/phs001502/phs001502.v1.p1/dbGaPEx2.1.5.xsdprimaryOK200GenomicCase-ControlUniversity.https://www.ncbi.nlm.nih.gov/projects/gap/cgi-bin/study.cgi?study_id=phs001502Sample Provider - Daniel J. Rader, MD - University of Pennsylvania, Philadelphia, PA, USAFunding Source - 5UM1HG008853 - National Institutes of Health, Bethesda, MD, USACo-Principal Investigators - Nathan O. Stitziel, MD, PhD - McDonnell Genome Institute, Washington University School of Medicine, St. Louis, MO, USACo-Principal Investigators - Susan K Dutcher, PhD - McDonnell Genome Institute, Washington University School of Medicine, St. Louis, MO, USAPrincipal Investigator - Ira M. Hall, PhD - McDonnell Genome Institute, Washington University School of Medicine, St. Louis, MO, USAdbGaPCardiovascular Disorders, other disease, scale tissue, ASCVD, Cardiovascular system disease, Other diseases of pericardium (disorder), Cardiovascular disease, acetylglucosaminyltransferase-like protein, Other pericardial disease NOS (disorder), peltate hair, Other heart disease (disorder), Other heart disease NOS (disorder), Cardiovascular disorder, Mbp1, PAPILLARY MUSCLE DIS NEC, Cardiac Event, Other diseases of pericardium, Other disorders of papillary muscle, Adverse, LARGE1, [X]Other specified diseases of pericardium (disorder), froggy, Gyltl1a, unspecified (disorder), Relative, Disorder of cardiovascular system (disorder), [X]Cardiovascular disease, Speciality, unspecified, Cardiac, Medical Specialities, Structural, diseases, Disease of cardiovascular system (disorder), Specialities, Other heart disease NOS, Functional, CVD, disease or disorder, diseases and disorders, DmF2, National Center for Human Genome Research (U.S.), myd, Fs(3)Hor, Other ill-defined heart disease NOS (disorder), Medical, Unspecified circulatory system disorder, lod, study, Cardiovascular Diseases, human disease, DmelCG2684, Other diseases of endocardium (disorder), Insurance Medicine, [X]Other specified diseases of pericardium, like-acetylglucosaminyltransferase, Genomes, MDDGB6, Comparative Genomics, plant peltate hair, [X]Other forms of heart disease (disorder), Other heart disease, Other ill-defined heart disease (disorder), Mbp-1, Age of onset, Other diseases of endocardium, Other forms of heart disease, LARGE, NTef2, circulatory system disease, Other specified pericardial disease NOS, non-neoplastic, genetic, cardiovascular disease, BPFD#36, drugs, Disorder of cardiovascular system, medicine, Medicine, disorder, Disease of cardiovascular system, Homo sapiens disease, Medicines, Insurance, constitutitional genetic, Event, Circulatory system disease NOS, OTHER SEQUELAE OF MI NEC, Circulatory system disease NOS (disorder), Disease, Specialties, Other ill-defined heart diseases, Genomics, gyltl1b-b, Medical Specialty, Comparative, not elsewhere classified, disorders, familial, Disorder of circulatory system, medical condition, Functional Genomics, Disease affecting entire cardiovascular system (disorder), Medical Specialties., Other ill-defined heart disease, disease of subdivision of hemolymphoid system, Fs(3)Sz11, Medical Speciality, Cardiac Events, NHGRI, MDDGA6, mKIAA0609, Relative Risks, Diseases, Adverse Cardiac Event, Specialty, condition, NOS, rare (European definition), Other pericardial disease NOS, scales, KIAA0609, Other forms of heart disease (disorder), Other ill-defined heart disease NOS, PERICARDIAL DISEASE NEC, acetylglucosaminyltransferase-like 1A, CIRCULATORY DISEASE NOS, CARDIOVASC DIS, Relative Risk, fg, Other specified diseases of pericardium, Cardiovascular, gyltl1b, scale, Risk, [X]Other ill-defined heart diseases, Risks, mdc1d, Adverse Cardiac Events, Disorder of the circulatory system, common, [X]Other forms of heart disease, [X]Other ill-defined heart diseases (disorder), whole genome, National Center for Human Genome Research, Age symptoms begin, Other sequelae of myocardial infarction, Lds, LARGE_HUMAN, early, Cardiovascular Disease, CVS disease, Phenotypes, Insurance Medicines, disease, MDC1D, Other specified pericardial disease NOS (disorder), like-glycosyltransferase, enr, Horka, National Human Genome Research Institute, ILL-DEFINED HRT DIS NEC, CG2684, Fs(3)Horka, Structural Genomics, inherited genetic, Major Adverse Cardiac Events, Disease affecting entire cardiovascular system, hereditary, glycosyltransferase-like protein LARGE1falseCCDG-Cardiovascular: University of Pennsylvania Cohort<p>The National Human Genome Research Institute (NHGRI) has funded the Centers for Common Disease Genomics (CCDG), a collaborative large-scale genome sequencing effort to comprehensively identify rare risk and protective variants contributing to multiple common disease phenotypes and to better understand the general principles of genomic architecture underlying common, complex inherited diseases.</p> <p>This study of early onset cardiovascular disease and metabolic risk contains data derived from the whole genome sequence data of individuals participating in Penn Medicine&#39;s BioBank. </p>2017-12-112017-12-11phs001502Cardiovascular Diseases