Trait
Abnormal blood clot
Clinical name: Abnormal thrombosis
Venous or arterial thrombosis (formation of blood clots) of spontaneous nature and which cannot be fully explained by acquired risk (e.g. atherosclerosis).
Summary
- Also called
- Abnormal blood clotting
Reference genomeGRCh38hg38
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Get my Genome Test19 genes linked to Abnormal blood clot
Changes in these genes cause rare conditions in which Abnormal blood clot 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 |
|---|---|---|
| BMPR2bone morphogenetic protein receptor type 2 | Often (30–79%) | In 1 condition |
| MPImannose phosphate isomerase | Often (30–79%) | In 2 conditions |
| RFT1RFT1 glycolipid translocator homolog | Often (30–79%) | In 1 condition |
| CALRcalreticulin | Sometimes (5–29%) | In 1 condition |
| F12coagulation factor XII | Sometimes (5–29%) | In 1 condition |
| JAK2Janus kinase 2 | Sometimes (5–29%) | In 2 conditions |
| MPLMPL proto-oncogene, thrombopoietin receptor | Sometimes (5–29%) | In 1 condition |
| MTHFRmethylenetetrahydrofolate reductase | Sometimes (5–29%) | In 1 condition |
| PIK3CAphosphatidylinositol-4,5-bisphosphate 3-kinase catalytic subunit alpha | Sometimes (5–29%) | In 1 condition |
| RHAGRh associated glycoprotein | Sometimes (5–29%) | In 1 condition |
| TET2tet methylcytosine dioxygenase 2 | Sometimes (5–29%) | In 1 condition |
| CFTRCF transmembrane conductance regulator | Not recorded | In 1 condition |
| CTRCchymotrypsin C | Not recorded | In 1 condition |
| HRGhistidine rich glycoprotein | Not recorded | In 1 condition |
| MYH9myosin heavy chain 9 | Not recorded | In 1 condition |
| PRSS1serine protease 1 | Not recorded | In 1 condition |
| PRSS2serine protease 2 | Not recorded | In 1 condition |
| SLC2A10solute carrier family 2 member 10 | Not recorded | In 1 condition |
| SPINK1serine peptidase inhibitor Kazal type 1 | 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.
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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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