Trait
Color vision test abnormality
Summary
- Also called
- Colour vision test abnormality
- Body system
- Abnormality of the eye
This page as data
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page$trait$nameRead the genes linked to Color vision test abnormality, and the rest of your genome, with one test.
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Get my Genome Test5 condition reports read genes linked to this trait
Dante Labs condition reports look at the genes behind groups of inherited conditions, read from one whole-genome test. Each page says which conditions and genes a report covers, how it is read and what it cannot tell you.
- AchromatopsiaReads 6 of these genesATF6CNGA3CNGB3GNAT2PDE6CPDE6HAbout this report →
- Colour Vision DeficiencyReads 1 of these genesOPN1SWAbout this report →
- Hereditary Spastic ParaplegiaReads 1 of these genesFA2HAbout this report →
- Retinitis PigmentosaReads 1 of these genesRPGRAbout this report →
Show 1 more report
Read the genes linked to Color vision test abnormality, and the rest of your genome, with one test.
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Get my Genome Test9 genes linked to Color vision test abnormality
Changes in these genes cause rare conditions in which Color vision test abnormality 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 |
|---|---|---|
| ATF6activating transcription factor 6 | Very often (80–99%) | In 1 condition |
| CNGA3cyclic nucleotide gated channel subunit alpha 3 | Very often (80–99%) | In 1 condition |
| CNGB3cyclic nucleotide gated channel subunit beta 3 | Very often (80–99%) | In 1 condition |
| GNAT2G protein subunit alpha transducin 2 | Very often (80–99%) | In 1 condition |
| PDE6Cphosphodiesterase 6C | Very often (80–99%) | In 1 condition |
| PDE6Hphosphodiesterase 6H | Very often (80–99%) | In 1 condition |
| RPGRretinitis pigmentosa GTPase regulator | Very often (80–99%) | In 1 condition |
| FA2Hfatty acid 2-hydroxylase | Often (30–79%) | In 1 condition |
| OPN1SWopsin 1, short wave sensitive | Often (30–79%) | 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 2026.10.19-9814e911.
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