Identification of Rare Variants in PD through Whole Exome Sequencing
Demographics (4)
- Age_Exam_Controls - Age of exam for controls (phv00226217.v1.p1)
- Age_Onset - Age of onset for cases (phv00226213.v1.p1)
- Sex - Subject gender (phv00226218.v1.p1)
- SEX - Subject gender (phv00226208.v1.p1)
Disease Events (1)
- AFFECTION_STATUS - Case control status for Parkinson disease (phv00226203.v1.p1)
Race and Ethnicity (2)
- Ethnicity - Ethnicity (phv00226215.v1.p1)
- Race - Race (phv00226214.v1.p1)
Other (15)
- ANALYTE_TYPE - Analyte type of the sample (phv00226221.v1.p1)
- BODY_SITE - Body part from which sample is collected (phv00226220.v1.p1)
- CAPTURE_KIT - Whole exome sequencing capture method (phv00226223.v1.p1)
- CONSENT - Subject consent group (phv00226202.v1.p1)
- FAMILY_ID - Unique, de-identified Family or Pedigree ID (phv00226204.v1.p1)
- FATHER - Unique, de-identified Father ID (phv00226206.v1.p1)
- IS_TUMOR - Tumor status of the sample (phv00226222.v1.p1)
- MOTHER - Unique, de-identified Mother ID (phv00226207.v1.p1)
- SAMPLE_ID - Unique, de-identified Sample ID (phv00226219.v1.p1)
- SAMPLE_ID - Unique, de-identified Sample ID (phv00226210.v1.p1)
- SAMPLE_USE - Sample Use (phv00226211.v1.p1)
- SUBJECT_ID - Unique, de-identified Subject ID (phv00226212.v1.p1)
- SUBJECT_ID - Unique, de-identified Subject ID (phv00226205.v1.p1)
- SUBJECT_ID - Unique, de-identified Subject ID (phv00226201.v1.p1)
- SUBJECT_ID - Unique, de-identified Subject ID (phv00226209.v1.p1)