Familial Exome Sequencing in Rare Pediatric Phenotypes
Anthropometry (2)
- height - Height measured at enrollment (phv00179537.v1.p1)
- weight - Subject's weight (phv00179542.v1.p1)
Demographics (2)
- age - Disease onset age (phv00179536.v1.p1)
- sex - Gender of participant (phv00179539.v1.p1)
Race and Ethnicity (1)
- race - Race of participant (phv00179540.v1.p1)
Other (25)
- AFFECTION_STATUS - Case control status of the subject (phv00179524.v1.p1)
- ANALYTE_TYPE - Analyte Type (phv00179545.v1.p1)
- birthplace - Place of subject's birth (phv00179538.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00179544.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00179521.v1.p1)
- education - Level of education (phv00179541.v1.p1)
- FAMID - Family ID (phv00179526.v1.p1)
- FATHER - Father's Subject ID (phv00179529.v1.p1)
- HISTOLOGICAL_TYPE - Cell or tissue type or subtype of sample (phv00179547.v1.p1)
- IS_TUMOR - Tumor status (phv00179546.v1.p1)
- MOTHER - Mother's Subject ID (phv00179528.v1.p1)
- POOLED_SAMPID - Sample ID created for pooled samples (phv00190929.v1.p1)
- POOLED_SUBJID - Subject ID created for pooled samples (phv00179525.v1.p1)
- SAMP_SOURCE - Source repository where samples originate (phv00179533.v1.p1)
- SAMPID - Sample ID (phv00179532.v1.p1)
- SAMPID - De-identified Sample ID (phv00179543.v1.p1)
- SAMPLE_USE - Sample use. SNP_Array: SNP genotypes obtained using standard or custom microarrays; WES_SRA: Whole exome sequencing data available through SRA (phv00190930.v1.p1)
- SEX - Sex (phv00179530.v1.p1)
- SOURCE_SAMPID - Sample ID used in the Source Repository (phv00179534.v1.p1)
- SOURCE_SUBJID - Subject ID used in the Source Repository (phv00179523.v1.p1)
- SUBJ_SOURCE - Source repository where subjects originate (phv00179522.v1.p1)
- SUBJID - De-identified Subject ID (phv00179535.v1.p1)
- SUBJID - Subject ID (phv00179520.v1.p1)
- SUBJID - Subject ID (phv00179531.v1.p1)
- SUBJID - Unique Subject ID (phv00179527.v1.p1)