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Hip shape mode 8

near LINC00415 · rs17083097

What the study found

Who was studied 38,175 European ancestry individuals, 5,310 East Asian ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.06 higher (95% confidence interval 0.04-0.08); p = 4 × 10−11.

How common The T allele had a frequency of about 16% in the people studied.

Where it sits Chromosome 13, band 13q12.13 — between genes, 10.7 kb from LINC00415.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Hip shape mode 8 — 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 shape mode 8.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Hip shape mode 8 compared to the general population.
Source

Questions about rs17083097

What is rs17083097?

rs17083097 is a single position in the genome, in or near the near LINC00415 gene. Published research associates it with hip shape mode 8. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs17083097 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 rs17083097 come from?

GWAS Catalog, Human molecular genetics 2025, PMID:39574169. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.

Hip shape mode 8 (rs17083097). MyGeneLog™. https://www.mygenelog.com/variants/rs17083097

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