NHLBI TOPMed: Boston-Brazil Sickle Cell Disease (SCD) Cohort
Biomarkers (5)
- HbA - Percent hemoglobin A (phv00492610.v1.p1)
- HbA2 - Percent hemoglobin A2 (phv00492611.v1.p1)
- HbC - Percent hemoglobin C (phv00492612.v1.p1)
- HbF - Percent fetal hemoglobin (phv00492613.v1.p1)
- HbS - Percent sickle hemoglobin (phv00492614.v1.p1)
Demographics (1)
- SEX - Gender of participant (phv00492601.v1.p1)
Other (26)
- ACS - Patient has experienced acute chest syndrome (phv00492615.v1.p1)
- AFFECTION_STATUS - Case control status of the subject for SCD (phv00492605.v1.p1)
- ANALYTE_TYPE - Analyte Type (phv00492623.v1.p1)
- AVN - Patient has experienced avascular necrosis (phv00492616.v1.p1)
- B_Genotype - Designation of the mutation present (phv00492606.v1.p1)
- BODY_SITE - Body site where sample was collected (phv00492622.v1.p1)
- BS_Haplotype - Beta-globin haplotype (phv00492607.v1.p1)
- CONSENT - Consent group as determined by DAC (phv00492600.v1.p1)
- Funding_Source - Project funding source (phv00492627.v1.p1)
- Hemoglobinopathy - Type of hemoglobinopathy (phv00492608.v1.p1)
- HISTOLOGICAL_TYPE - Cell or tissue type or subtype of sample (phv00492625.v1.p1)
- HU_Treatment - Patient has been treated with hydroxyurea (phv00492620.v1.p1)
- IS_TUMOR - Tumor status (phv00492624.v1.p1)
- Leg_Ulcer - Patient has experienced a leg ulcer (phv00492617.v1.p1)
- Priapism - Presence of priapism (phv00492618.v1.p1)
- SAMPLE_ID - De-identified Sample ID (phv00492621.v1.p1)
- SAMPLE_ID - Sample ID (phv00492603.v1.p1)
- SEQUENCING_CENTER - Name of the center which conducted sequencing (phv00492626.v1.p1)
- Stroke - Patient has experienced a stroke (phv00492619.v1.p1)
- Study_Name - TOPMed-assigned short study name (1:1 with TOPMed phs number) (phv00492630.v1.p1)
- SUBJECT_ID - De-identified Subject ID (phv00492604.v1.p1)
- SUBJECT_ID - Subject ID (phv00492599.v1.p1)
- SUBJECT_ID - Subject ID (phv00492602.v1.p1)
- TOPMed_Phase - TOPMed Phase (phv00492628.v1.p1)
- TOPMed_Project - TOPMed Project that funded sequencing (phv00492629.v1.p1)
- Xmn_I - Xmn I polymorphism (phv00492609.v1.p1)