UW-CMG: Atrioventricular Septal Defects (AVSD) Study
Ancestry (1)
- ANCESTRY - Ancestry of the subject (phv00404332.v1.p1)
Demographics (2)
- SEX - Subject's gender (phv00404331.v1.p1)
- SEX - Subject's gender (phv00404323.v1.p1)
Disease Events (1)
- AFFECTION_STATUS - Case control status of the subject for Atrioventricular Septal Defects (AVSD) (phv00404334.v1.p1)
Other (17)
- ANALYTE_TYPE - Analyte Type (phv00404338.v1.p1)
- CONDITION - Name of disorder; presumed or confirmed. (phv00404333.v1.p1)
- CONSANGUINITY - Consanguinity relative to parents (phv00404335.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00404316.v1.p1)
- FAMID - Family ID (phv00404320.v1.p1)
- FATHER - Father's Subject ID, which is de-identified (phv00404322.v1.p1)
- MOTHER - Mother's Subject ID, which is de-identified (phv00404321.v1.p1)
- OMIM_ID - Phenotype ID from Online Mendelian Inheritance in Man (phv00404336.v1.p1)
- SAMPLE_ID - De-identified sequence lab ID of the sample. (phv00404326.v1.p1)
- SAMPLE_ID - De-identified sequence lab ID of the sample. (phv00404337.v1.p1)
- SAMPLE_SOURCE - Source repository (phv00404327.v1.p1)
- SOURCE_SAMPLE_ID - Sample ID used in the source repository (phv00404328.v1.p1)
- SUBJID - Sequence Lab ID number, which is de-identified and unique (phv00404330.v1.p1)
- SUBJID - Sequence Lab ID number, which is de-identified and unique (phv00404319.v1.p1)
- SUBJID - Sequence Lab ID number, which is de-identified and unique (phv00404325.v1.p1)
- SUBJID - Subject ID (phv00404315.v1.p1)
- TWIN_ID - Designates MZ twins (phv00404324.v1.p1)