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Hip minimal joint space width

MYPOP · rs34717890

What the study found

Who was studied 50,745 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.1 higher (95% confidence interval 0.08-0.12); p = 1 × 10−27.

How common The T allele had a frequency of about 12% in the people studied.

Where it sits Chromosome 19, band 19q13.32 — in an intron of MYPOP.

What each result means

C/C No copy of the version the research linked to Hip minimal joint space width. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Hip minimal joint space width. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Hip minimal joint space width. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs34717890

What is rs34717890?

rs34717890 is a single position in the genome, in or near the MYPOP 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 rs34717890 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 rs34717890 come from?

GWAS Catalog, EBioMedicine 2023, PMID:37619450. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Hip minimal joint space width (rs34717890). MyGeneLog™. https://www.mygenelog.com/variants/rs34717890

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