Reference genomeGRCh38hg38
Positions on gene and variant pages follow this choice, in this browser.
Read the genes linked to Abnormal best corrected visual acuity test, and the rest of your genome, with one test.
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Get my Genome Test7 genes linked to Abnormal best corrected visual acuity test
Changes in these genes cause rare conditions in which Abnormal best corrected visual acuity test 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 |
|---|---|---|
| C1QTNF5C1q and TNF related 5 | Very often (80–99%) | In 1 condition |
| COL25A1collagen type XXV alpha 1 chain | Very often (80–99%) | In 1 condition |
| KIF21Akinesin family member 21A | Very often (80–99%) | In 1 condition |
| PHOX2Apaired like homeobox 2A | Very often (80–99%) | In 1 condition |
| TUBA1Atubulin alpha 1a | Very often (80–99%) | In 1 condition |
| TUBB2Btubulin beta 2B class IIb | Very often (80–99%) | In 1 condition |
| TUBB3tubulin beta 3 class III | Very often (80–99%) | In 2 conditions |
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.
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