Trait
Broad collarbone
Clinical name: Broad clavicle
Increased width (cross-sectional diameter) of the clavicles.
Summary
- Also called
- Broad clavicles
- Body system
- Abnormality of the musculoskeletal system
Reference genomeGRCh38hg38
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Get my Genome Test11 genes linked to Broad collarbone
Changes in these genes cause rare conditions in which Broad collarbone 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 |
|---|---|---|
| ARSKarylsulfatase family member K | Always | In 1 condition |
| PTDSS1phosphatidylserine synthase 1 | Always | In 1 condition |
| PTH1Rparathyroid hormone 1 receptor | Very often (80–99%) | In 1 condition |
| MMP14matrix metallopeptidase 14 | Often (30–79%) | In 1 condition |
| MMP2matrix metallopeptidase 2 | Often (30–79%) | In 1 condition |
| WNT7AWnt family member 7A | Often (30–79%) | In 1 condition |
| MYSM1Myb like, SWIRM and MPN domains 1 | Sometimes (5–29%) | In 1 condition |
| ATP7AATPase copper transporting alpha | Not recorded | In 1 condition |
| SH3PXD2BSH3 and PX domains 2B | Not recorded | In 1 condition |
| SOSTsclerostin | Not recorded | In 1 condition |
| TRIP11thyroid hormone receptor interactor 11 | 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.
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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