Whole Genome Sequencing to Identify Causal Genetic Variants Influencing CVD Risk - San Antonio Family Studies
| Short Name | SAFS
|
|---|---|
| Institution(s) |
University of Texas Rio Grande Valley School of Medicine
|
| Type of Omics | WGS
|
| Approx. Sample Size | 1142 |
| Disease/Phenotype |
cardiometabolic risk factors
|
| Starting Phase | Phase 1
|
| TOPMed Accession # |
phs001215
|
| Omics Center(s) Phase 1 |
Illumina
|
| Specify the TOPMed Phase for the Omics Center(s) selected above |
legacy
|
| Phases Involved |
1
|
| Populations |
Mexican American in SAFHS extended pedigrees
|
| PI | |
| Co-PI | |
| Contact | |
| Phenotype Liaison | |
| Data Set contact(s) | |
| Project |
SAFS
|
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