Genetics of COVID-19 Susceptibility and Manifestations
NCT04371432 · Status: COMPLETED · Type: OBSERVATIONAL · Enrollment: 721
Last updated 2026-05-01
Summary
Background:
Coronavirus 2019 (COVID-19, or SARS-CoV-2) is a serious public health problem, and genetics may play a role in how serious the illness becomes in certain people. Genes are the instructions that our body uses to grow and develop. Variations in our genes can cause medical conditions and may be the reason why some people get sicker than others.
Objective:
This study aims to learn more about the genetic contributions to the severity of COVID-19. We hope to use this information to develop therapies that reduce the severity of COVID-19 symptoms in some people.
Eligibility:
Anyone located in the United States who has tested positive for SARS-CoV-2 infection may be eligible to join (including NIH staff).
Design:
Participants will complete a questionnaire about their health history and COVID-19 symptoms.
Participants will give a blood or saliva sample. It will be about 2 tablespoons of blood, or we will send a saliva collection kit. Researchers will use this blood or saliva sample to study the participant s DNA.
The data about participants genes will be stored in a large database. The database will be shared with other qualified researchers who are trying to learn about COVID-19. Participants names and other personal details will not be shared. Instead, the data will be labeled with a code.
Participants may be contacted by study team members for up to a year after they join the study.
Conditions
- COVID-19
- Coronavirus 2019
Sponsors & Collaborators
-
National Human Genome Research Institute (NHGRI)
lead NIH
Principal Investigators
-
Leslie G Biesecker, M.D. · National Human Genome Research Institute (NHGRI)
Eligibility
- Min Age
- 1 Month
- Max Age
- 110 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2020-05-05
- Primary Completion
- 2021-11-23
- Completion
- 2024-12-15
Countries
- United States
Study Locations
More Related Trials
-
Immunogenetics Predictors With COVID-19
NCT04390269 ·Status: UNKNOWN
-
Genetic Bases of COVID-19 Clinical Variability
NCT04549831 ·Status: RECRUITING
-
The Fondazione Genomic SARS-CoV-2 Study COVID-19
NCT06549712 ·Status: COMPLETED ·Phase: NA
-
Identification of Genetic Factors Determining Disease Course in the New Type of Coronavirus Infection, COVID-19
NCT04426253 ·Status: UNKNOWN
-
Next Generation to Identify Genetic Causes of Disease in Patients Participating in NICHD Clinical Protocols
NCT01375543 ·Status: COMPLETED
-
Use of Population Descriptors in Human Genetic Research
NCT00767702 ·Status: COMPLETED
-
Identification and Characterization of Novel Non-Coding Variants That Contribute to Genetic Disorders
NCT04399694 ·Status: COMPLETED
-
Genetic Data Collection in Adult Participants to Identify Genetic Variants of Known Importance in Non-alcoholic Steatohepatitis (NASH)
NCT05423327 ·Status: TERMINATED ·Phase: NA
-
Development and Validation of a Model to Predict Fast Progression in Glaucoma
NCT04454190 ·Status: TERMINATED
-
Investigating the Feasibility and Implementation of Whole Genome Sequencing in Patients With Suspected Genetic Disorder
NCT03829176 ·Status: COMPLETED ·Phase: NA
-
Cultural Congruence in International Genetics Research
NCT00767858 ·Status: TERMINATED
-
Patients' Perspectives on Identity, Ancestry and Genetics
NCT00359710 ·Status: COMPLETED
-
The Role of Genetic Polymorphisms in Innate Immune Response Genes in Susceptibility to Infections
NCT00597090 ·Status: COMPLETED
-
Impact of the Genetic Polymorphism on COVID-19 in Egypt
NCT05157217 ·Status: UNKNOWN
-
Observational Study of Advanced Data Analytics in Genetic Conditions
NCT05657405 ·Status: RECRUITING
-
Analysis of Genes That Predispose People to Develop High Blood Pressure
NCT00522119 ·Status: COMPLETED
-
Reverse Phenotyping Core
NCT03632239 ·Status: ENROLLING_BY_INVITATION
-
Genetics of Hepatitis C Virus Infection
NCT00005657 ·Status: COMPLETED
-
Genetic Susceptibility to Severe Infections
NCT06102070 ·Status: RECRUITING
-
Trial of Preemptive Pharmacogenetics in Underserved Patients
NCT05141019 ·Status: ACTIVE_NOT_RECRUITING ·Phase: NA
-
Brain Genomics Superstruct Project
NCT01552460 ·Status: COMPLETED
-
Physicians' Understanding of Human Genetic Variation
NCT00339924 ·Status: COMPLETED
-
Genetic Analysis of Uncommon Disease Presentations in Non-US Populations
NCT06595940 ·Status: RECRUITING
-
Study of the Genome, Gut Metagenome and Diet of Patients With Incident Parkinson's Disease
NCT04119596 ·Status: TERMINATED
-
Is Family Screening Improved by Genetic Testing of Familial Hypercholesterolemia
NCT04526457 ·Status: COMPLETED ·Phase: NA