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Hip minimal joint space width

RUNX2 · rs10948155

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Hip minimal joint space width — no copies of the reported risk allele. (GWAS Catalog, PLoS Genet 2016, PMID:27701424)

C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Hip minimal joint space width. (GWAS Catalog, PLoS Genet 2016, PMID:27701424)

T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Hip minimal joint space width compared to the general population. (GWAS Catalog, PLoS Genet 2016, PMID:27701424)

Source: GWAS Catalog, PLoS Genet 2016, PMID:27701424

Questions about rs10948155

What is rs10948155?

rs10948155 is a single position in the genome, in or near the RUNX2 gene. Published research associates it with hip minimal joint space width. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10948155 mean I will get this?

No. Common variants like this one move a probability slightly and, on their own, rarely decide anything about one person. Nothing on this page is a diagnosis, and health decisions should be made with a clinician who can see your whole picture.

Where does the information about rs10948155 come from?

GWAS Catalog, PLoS Genet 2016, PMID:27701424. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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