Trait
Low blood pressure
Clinical name: Hypotension
Low Blood Pressure, vascular hypotension.
Summary
- Also called
- Arterial hypotension
- Body system
- Abnormality of the cardiovascular system
Reference genomeGRCh38hg38
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Get my Genome Test74 genes linked to Low blood pressure
Changes in these genes cause rare conditions in which Low blood pressure 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 |
|---|---|---|
| HADHBhydroxyacyl-CoA dehydrogenase trifunctional multienzyme complex subunit beta | Always | In 1 condition |
| OTULINOTU deubiquitinase with linear linkage specificity | Always | In 1 condition |
| RAB32RAB32, member RAS oncogene family | Always | In 1 condition |
| SCNN1Asodium channel epithelial 1 subunit alpha | Always | In 1 condition |
| SERPINA6serpin family A member 6 | Always | In 1 condition |
| TNNT2troponin T2, cardiac type | Always | In 1 condition |
| CYP11A1cytochrome P450 family 11 subfamily A member 1 | Very often (80–99%) | In 2 conditions |
| CYP11B2cytochrome P450 family 11 subfamily B member 2 | Very often (80–99%) | In 2 conditions |
| MC2Rmelanocortin 2 receptor | Very often (80–99%) | In 1 condition |
| MRAPmelanocortin 2 receptor accessory protein | Very often (80–99%) | In 1 condition |
| NFKB2nuclear factor kappa B subunit 2 | Very often (80–99%) | In 1 condition |
| NNTnicotinamide nucleotide transhydrogenase | Very often (80–99%) | In 1 condition |
| SAA1serum amyloid A1 | Very often (80–99%) | In 1 condition |
| SIM1SIM bHLH transcription factor 1 | Very often (80–99%) | In 1 condition |
| SLC25A20solute carrier family 25 member 20 | Very often (80–99%) | In 2 conditions |
| STARsteroidogenic acute regulatory protein | Very often (80–99%) | In 1 condition |
| TBX19T-box transcription factor 19 | Very often (80–99%) | In 1 condition |
| TXNRD2thioredoxin reductase 2 | Very often (80–99%) | In 1 condition |
| AAASaladin WD repeat nucleoporin | Often (30–79%) | In 1 condition |
| AIPAHR interacting HSP90 co-chaperone | Often (30–79%) | In 1 condition |
| ASXL1ASXL transcriptional regulator 1 | Often (30–79%) | In 2 conditions |
| CASRcalcium sensing receptor | Often (30–79%) | In 1 condition |
| CBLCbl proto-oncogene | Often (30–79%) | In 1 condition |
| CD4CD4 molecule | Often (30–79%) | In 1 condition |
| CDH23cadherin related 23 | Often (30–79%) | In 2 conditions |
| FOXA2forkhead box A2 | Often (30–79%) | In 1 condition |
| GLI2GLI family zinc finger 2 | Often (30–79%) | In 1 condition |
| GMPPAGDP-mannose pyrophosphorylase A | Often (30–79%) | In 1 condition |
| GNA11G protein subunit alpha 11 | Often (30–79%) | In 1 condition |
| HESX1HESX homeobox 1 | Often (30–79%) | In 1 condition |
| HSD3B2hydroxy-delta-5-steroid dehydrogenase, 3 beta- and steroid delta-isomerase 2 | Often (30–79%) | In 1 condition |
| IRF4interferon regulatory factor 4 | Often (30–79%) | In 1 condition |
| KYNUkynureninase | Often (30–79%) | In 1 condition |
| LHX4LIM homeobox 4 | Often (30–79%) | In 1 condition |
| MEN1menin 1 | Often (30–79%) | In 1 condition |
| MMACHCmetabolism of cobalamin associated C | Often (30–79%) | In 1 condition |
| OTX2orthodenticle homeobox 2 | Often (30–79%) | In 1 condition |
| POU1F1POU class 1 homeobox 1 | Often (30–79%) | In 1 condition |
| PRDX1peroxiredoxin 1 | Often (30–79%) | In 1 condition |
| PRKAG2protein kinase AMP-activated non-catalytic subunit gamma 2 | Often (30–79%) | In 1 condition |
Show 34 more genes
| Gene | How often it is seen | Conditions |
|---|---|---|
| PROP1PROP paired-like homeobox 1 | Often (30–79%) | In 2 conditions |
| RUNX1RUNX family transcription factor 1 | Often (30–79%) | In 1 condition |
| SOX3SRY-box transcription factor 3 | Often (30–79%) | In 1 condition |
| SRSF2serine and arginine rich splicing factor 2 | Often (30–79%) | In 2 conditions |
| TET2tet methylcytosine dioxygenase 2 | Often (30–79%) | In 2 conditions |
| TRAPPC11trafficking protein particle complex subunit 11 | Often (30–79%) | In 1 condition |
| ABCA3ATP binding cassette subfamily A member 3 | Sometimes (5–29%) | In 1 condition |
| ACAT1acetyl-CoA acetyltransferase 1 | Sometimes (5–29%) | In 1 condition |
| CD46CD46 molecule | Sometimes (5–29%) | In 1 condition |
| CFHcomplement factor H | Sometimes (5–29%) | In 1 condition |
| CFIcomplement factor I | Sometimes (5–29%) | In 1 condition |
| DCTN1dynactin subunit 1 | Sometimes (5–29%) | In 1 condition |
| DDCdopa decarboxylase | Sometimes (5–29%) | In 2 conditions |
| FMR1fragile X messenger ribonucleoprotein 1 | Sometimes (5–29%) | In 1 condition |
| HELLPARHELLP associated long non-coding RNA | Sometimes (5–29%) | In 1 condition |
| HMGCL3-hydroxy-3-methylglutaryl-CoA lyase | Sometimes (5–29%) | In 1 condition |
| KITKIT proto-oncogene, receptor tyrosine kinase | Sometimes (5–29%) | In 2 conditions |
| PDE4Dphosphodiesterase 4D | Sometimes (5–29%) | In 1 condition |
| RYR1ryanodine receptor 1 | Sometimes (5–29%) | In 2 conditions |
| SERPING1serpin family G member 1 | Sometimes (5–29%) | In 1 condition |
| SFTPBsurfactant protein B | Sometimes (5–29%) | In 1 condition |
| SFTPCsurfactant protein C | Sometimes (5–29%) | In 1 condition |
| ATRXATRX chromatin remodeler | Rarely (1–4%) | In 1 condition |
| ACEangiotensin I converting enzyme | Not recorded | In 1 condition |
| AGTangiotensinogen | Not recorded | In 1 condition |
| AGTR1angiotensin II receptor type 1 | Not recorded | In 1 condition |
| ALBalbumin | Not recorded | In 1 condition |
| CLCNKBchloride voltage-gated channel Kb | Not recorded | In 1 condition |
| MUC1mucin 1, cell surface associated | Not recorded | In 1 condition |
| NR3C2nuclear receptor subfamily 3 group C member 2 | Not recorded | In 1 condition |
| RENrenin | Not recorded | In 1 condition |
| SCNN1Bsodium channel epithelial 1 subunit beta | Not recorded | In 1 condition |
| SLC12A3solute carrier family 12 member 3 | Not recorded | In 1 condition |
| VHLvon Hippel-Lindau tumor suppressor | 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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