Trait
Persistent EBV viremia
Persistent or recurrent detection of Epstein-Barr virus (EBV) in the blood that occurs in the context of unusual susceptibility to infection.
Summary
- Also called
- Chronic EBV viremia, Persistent EBV viraemia, Recurrent EBV viremia
Read the genes linked to Persistent EBV viremia, and the rest of your genome, with one test.
From $449Free shipping · Results in 6–8 weeks
Get my Genome Test19 genes linked to Persistent EBV viremia
Changes in these genes cause rare conditions in which Persistent EBV viremia is seen. Most people with this trait have none of those conditions, and a gene on this list says nothing about anyone's own genome.
| Gene | How often it is seen | Conditions |
|---|---|---|
| CD28CD28 molecule | Always | In 1 condition |
| IRF4interferon regulatory factor 4 | Always | In 1 condition |
| ITKIL2 inducible T cell kinase | Always | In 1 condition |
| ITPR3inositol 1,4,5-trisphosphate receptor type 3 | Always | In 1 condition |
| MAGT1magnesium transporter 1 | Always | In 1 condition |
| PRKCDprotein kinase C delta | Always | In 1 condition |
| TNFRSF9TNF receptor superfamily member 9 | Always | In 1 condition |
| CD27CD27 molecule | Often (30–79%) | In 1 condition |
| DEF6DEF6 guanine nucleotide exchange factor | Often (30–79%) | In 1 condition |
| FLT3LGfms related receptor tyrosine kinase 3 ligand | Often (30–79%) | In 1 condition |
| IKZF3IKAROS family zinc finger 3 | Often (30–79%) | In 1 condition |
| IL27RAinterleukin 27 receptor subunit alpha | Often (30–79%) | In 1 condition |
| LATlinker for activation of T cells | Often (30–79%) | In 1 condition |
| PGM3phosphoglucomutase 3 | Often (30–79%) | In 1 condition |
| STK4serine/threonine kinase 4 | Often (30–79%) | In 1 condition |
| TET2tet methylcytosine dioxygenase 2 | Often (30–79%) | In 1 condition |
| TOM1target of myb1 membrane trafficking protein | Often (30–79%) | In 1 condition |
| TRACT cell receptor alpha constant | Often (30–79%) | In 1 condition |
| PIK3R1phosphoinositide-3-kinase regulatory subunit 1 | Sometimes (5–29%) | In 1 condition |
How often is among people with one of the gene's conditions, the most often across them, as the Human Phenotype Ontology records it. These pages describe traits and the research behind them; they are not a diagnosis, and a doctor or genetic counsellor is the person to ask about symptoms.
Broader traits
Where this comes from
- The Human Phenotype Ontology, release 2026-09-01: the trait, its names, its definition and the genes linked to it. Find out more at hpo.jax.org.
- Data release 2026.10.16-c6eea6bf.
One test. A lifetime of answers.
From $449Free shipping · Results in 6–8 weeks