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Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
ChillsHP:0025143
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Get my Genome Test19 genes linked to Chills
Changes in these genes cause rare conditions in which Chills 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 |
|---|---|---|
| HAVCR2hepatitis A virus cellular receptor 2 | Often (30–79%) | In 1 condition |
| MVKmevalonate kinase | Often (30–79%) | In 1 condition |
| ANK1ankyrin 1 | Sometimes (5–29%) | In 1 condition |
| CD28CD28 molecule | Sometimes (5–29%) | In 1 condition |
| CTLA4cytotoxic T-lymphocyte associated protein 4 | Sometimes (5–29%) | In 1 condition |
| EPB42erythrocyte membrane protein band 4.2 | Sometimes (5–29%) | In 1 condition |
| PKHD1PKHD1 ciliary IPT domain containing fibrocystin/polyductin | Sometimes (5–29%) | In 1 condition |
| SLC4A1solute carrier family 4 member 1 (Diego blood group) | Sometimes (5–29%) | In 1 condition |
| SPTA1spectrin alpha, erythrocytic 1 | Sometimes (5–29%) | In 2 conditions |
| SPTBspectrin beta, erythrocytic | Sometimes (5–29%) | In 2 conditions |
| TBK1TANK binding kinase 1 | Sometimes (5–29%) | In 1 condition |
| TICAM1TIR domain containing adaptor molecule 1 | Sometimes (5–29%) | In 1 condition |
| TLR3toll like receptor 3 | Sometimes (5–29%) | In 1 condition |
| TNFRSF1BTNF receptor superfamily member 1B | Sometimes (5–29%) | In 1 condition |
| TRAF3TNF receptor associated factor 3 | Sometimes (5–29%) | In 1 condition |
| UNC93B1unc-93B1 regulator of TLR signaling | Sometimes (5–29%) | In 1 condition |
| EPB41erythrocyte membrane protein band 4.1 | Rarely (1–4%) | In 1 condition |
| GYPCglycophorin C (Gerbich blood group) | Rarely (1–4%) | In 1 condition |
| NLRP3NLR family pyrin domain containing 3 | Not recorded | 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.
Narrower traits
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.
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