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Hip bone size

near RPS20P12 · rs7575512

What the study found

Who was studied 3,267 European ancestry individuals, 1,619 Chinese ancestry individuals, 843 African American individuals, 446 Hispanic individuals.

The effect Each copy of the T allele shifted the measure 0.13 higher (95% confidence interval 0.091-0.169); p = 3 × 10−10.

Where it sits Chromosome 2, band 2q37.1 — between genes, 27.8 kb from RPS20P12.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Hip bone size — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Hip bone size.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Hip bone size compared to the general population.
Source

Questions about rs7575512

What is rs7575512?

rs7575512 is a single position in the genome, in or near the near RPS20P12 gene. Published research associates it with hip bone size. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs7575512 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 rs7575512 come from?

GWAS Catalog, Osteoporosis international : a journal established as result of cooperation between the European Foundation for Osteoporosis and the National Osteoporosis Foundation of the USA 2020, PMID:32314116. 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 bone size (rs7575512). MyGeneLog™. https://www.mygenelog.com/variants/rs7575512

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