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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 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 0.07 higher (95% confidence interval 0.05-0.09); p = 2 × 10−24.
How common The T allele had a frequency of about 30% in the people studied.
Where it sits Chromosome 12, band 12p11.22 — in an intron of CCDC91.
What each result means
C/CNo copy of the version the research linked to Hip shape mode 9. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Hip shape mode 9. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Hip shape mode 9. That is the strongest link of the three results. A link in a study is not a diagnosis.
Human molecular genetics · 2025 · PMID 39574169 · open access
Questions about rs11049418
What is rs11049418?
rs11049418 is a single position in the genome, in or near the CCDC91 gene. Published research associates it with hip shape mode 9. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs11049418 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 rs11049418 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.
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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 9 (rs11049418). MyGeneLog™. https://www.mygenelog.com/variants/rs11049418