Rare Germline Variations in Familial Melanoma
Demographics (2)
- SEX - Gender of participant (phv00265767.v2.p1)
- SEX - Gender of participant (phv00278184.v1.p1)
Disease Events (1)
- AFFECTION_STATUS - Affected status of the subject for Melanoma (phv00420922.v1.p1)
Other (18)
- ANALYTE_TYPE - Analyte Type (phv00265772.v2.p1)
- BODY_SITE - Body site where sample was collected (phv00265771.v2.p1)
- CONSENT - Consent (phv00265761.v2.p1)
- DISPLAYED_FAMILY_ID - Family ID as displayed in the published paper (phv00278187.v2.p1)
- DISPLAYED_SUBJECT_ID - Subject ID as displayed in the published paper (phv00278188.v2.p1)
- FAMILY_ID - De-identified Family ID (phv00278185.v2.p1)
- FAMILY_ID - De-identified Family ID (phv00278180.v1.p1)
- FATHER - Father's de-identified Subject ID (phv00278183.v1.p1)
- HISTOLOGICAL_TYPE - Histological Type (phv00265770.v2.p1)
- IS_TUMOR - Tumor status (phv00265773.v2.p1)
- MOTHER - Mother's de-identified Subject ID (phv00278182.v1.p1)
- RELATIONSHIP - PROBAND or relationship to the PROBAND of the family (phv00278186.v2.p1)
- SAMPLE_ID - De-identified Sample ID (phv00265769.v2.p1)
- SAMPLE_ID - De-identified Sample ID (phv00265764.v2.p1)
- SUBJECT_ID - De-identified Subject ID (phv00265766.v2.p1)
- SUBJECT_ID - De-identified Subject ID (phv00278181.v1.p1)
- SUBJECT_ID - De-identified Subject ID (phv00265760.v2.p1)
- SUBJECT_ID - De-identified Subject ID (phv00265763.v2.p1)