<p>This substudy phs000307 Framingham Allelic Spectrum Project includes the generation of deep coverage targeted re-sequencing and variant identification for 216 genes in the Framingham Heart Study (FHS) sample collection, produced  as part of NHLBI's Medical Resequencing projects. Summary level phenotypes for the Framingham Cohort study participants can be viewed at the</p>

Framingham Heart Study Allelic Spectrum Project

Cardiovascular Diseases study with SNP/CNV Genotypes (NGS), WXS data on BDC (1,623 participants)