Whole Genome Sequencing to Identify Causal Genetic Variants Influencing CVD Risk - San Antonio Family Studies

Institution(s): 
University of Texas Rio Grande Valley School of Medicine
Approx. Sample Size: 
1142
Populations: 

Mexican American in SAFHS extended pedigrees

Project:

Disease/Phenotype: 

cardiometabolic risk factors

PI: 
John Blangero
Omics Center(s) Phase 1: 
Illumina
NIH Program Officer: 
Starting Phase: 
Phase 1
Phases Involved: 
1
Co-PI: 
Joanne Curran
Phenotype Liaison: 
Short Name: 
SAFS
Type of Omics: 
WGS
External Funding: 
TOPMed Accession #: 
Omics Center(s) Other Phase (specify): 
Illumina
Specify the TOPMed Phase for the Omics Center(s) selected above: 
legacy