NINDS Family-Based Whole-Genome Sequencing to Find HD Modifiers
Demographics (4)
- age_assessed - Subject age at last assessment (phv00259736.v1.p1)
- age_onset - Disease onset age (phv00259735.v1.p1)
- sex - Gender of participant (phv00259737.v1.p1)
- SEX - Sex (phv00259729.v1.p1)
Disease Events (1)
- AFFECTION_STATUS - Case - control status (HD) of the subject (phv00259724.v1.p1)
Race and Ethnicity (1)
- race - Race of participant (phv00259738.v1.p1)
Other (17)
- affected - Individual has HD or not at time of assessment (phv00259734.v1.p1)
- ANALYTE_TYPE - Analyte Type (phv00259743.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00259742.v1.p1)
- CAG_repeat_size_1 - CAG repeat size from one allele (major) (phv00259739.v1.p1)
- CAG_repeat_size_2 - CAG repeat size from one allele (minor) (phv00259740.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00259723.v1.p1)
- FAMILY_ID - Family ID (phv00259725.v1.p1)
- FATHER - Father's Subject ID (phv00259727.v1.p1)
- MOTHER - Mother's Subject ID (phv00259728.v1.p1)
- SAMPLE_ID - De-identified Sample ID (phv00259741.v1.p1)
- SAMPLE_ID - Sample ID (phv00259731.v1.p1)
- SAMPLE_USE - Sample use. Seq_DNA_SNP_CNV: SNP and CNV genotypes derived from sequence data; Seq_DNA_WholeGenome: Whole genome sequencing (phv00259732.v1.p1)
- SEQUENCING_CENTER - Name of the center which conducted sequencing (phv00259744.v1.p1)
- SUBJECT_ID - De-identified Subject ID (phv00259733.v1.p1)
- SUBJECT_ID - Unique Subject ID (phv00259726.v1.p1)
- SUBJECT_ID - Subject ID (phv00259722.v1.p1)
- SUBJECT_ID - Subject ID (phv00259730.v1.p1)