NHLBI Framingham SNP Health Association Resource (SHARe)
Demographics (2)
- DAYS_POSTEX1_OF_DNA_DRAW - NUMBER OF DAYS BETWEEN EXAM1 AND DNA DRAW DATE (phv00480075.v4.p16)
- EXAM - Exam from which sample was collected (phv00536849.v2.p16)
Study Administration (1)
- IDTYPE - Framingham Heart Study cohort identifier (phv00480074.v4.p16)
Other (25)
- ADD_DIAB_SNPS - Genotypes of rare variants in genomic regions associated with risk of type 2 diabetes (T2D) or diabetes related quantitative traits that are not part of extant genotyped or imputed GWAS data in Framingham Heart Study cohorts (phv00221187.v7.p16)
- ANALYTE_TYPE - Analyte type - all DNA (phv00173528.v9.p16)
- ANALYTE_TYPE - Analyte Type (phv00536847.v2.p16)
- ANALYTE_TYPE - Analyte Type (phv00504353.v3.p16)
- ANALYTE_TYPE - Analyte Type (phv00504357.v1.p16)
- ANALYTE_TYPE - Analyte Type (phv00536852.v1.p16)
- BODY_SITE - Body site - values include blood, cell line, or serum (phv00173526.v9.p16)
- BODY_SITE - Body site where sample was collected (phv00536846.v2.p16)
- BODY_SITE - Body site where sample was collected (phv00504352.v3.p16)
- BODY_SITE - Body site where sample was collected (phv00504356.v1.p16)
- BODY_SITE - Body site where sample was collected (phv00536851.v1.p16)
- high_flag - Value equals 1 for the unique sample to be used (useful if multiple samples from the same subject are present) in the original SHARe genotyping; value equals 2 for the unique samples with OMNI5.0 chip genotyping (phv00173525.v9.p16)
- IS_TUMOR - Tumor status (phv00536848.v2.p16)
- IS_TUMOR - Tumor status (phv00504354.v3.p16)
- IS_TUMOR - Tumor status (phv00504358.v1.p16)
- IS_TUMOR - Tumor status (phv00536853.v1.p16)
- plate_well - The well designation in AFFYMETRIX and Illumina production manifests (phv00173524.v9.p16)
- SAMPLE_ID - Sample ID - SHARe genotyped sample ID (phv00173523.v9.p16)
- SAMPLE_ID - Sample ID (phv00536845.v2.p16)
- SAMPLE_ID - Sample ID (phv00504351.v3.p16)
- SAMPLE_ID - Sample ID (phv00504355.v1.p16)
- SAMPLE_ID - Sample ID (phv00536850.v1.p16)
- shareid - Unique study participant identification number (phv00480073.v4.p16)
- shareid - SHARe ID number (phv00221186.v7.p16)
- WGA - This has a value of 1 in cases where DNA was amplified. A subset of the blood samples were amplified for SHARe; none for OMNI5.0; all serum samples were amplified in SHARe. (phv00173527.v9.p16)