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Who was studied 9,103 South Indian ancestry individuals.
The effect
Each copy of the G allele shifted the measure 1.44 higher (95% confidence interval 0.93-1.95); p = 3 × 10−8.
How common The G allele had a frequency of about 9% in the people studied.
Where it sits Chromosome 10, band 10q26.12 — in an intron of LINC02930.
What each result means
A/ANo copy of the version the research linked to Type 2 diabetes (age of onset). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Type 2 diabetes (age of onset). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Type 2 diabetes (age of onset). That is the strongest link of the three results. A link in a study is not a diagnosis.
Diabetes care · 2023 · PMID 37308106 · open access
Questions about rs3011366
What is rs3011366?
rs3011366 is a single position in the genome, in or near the near WDR11 gene. Published research associates it with type 2 diabetes (age of onset). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs3011366 linked to?
On MyGeneLog this position is linked to Type 2 Diabetes. The research behind each link, and its sources, are set out on that condition page.
Does having rs3011366 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 rs3011366 come from?
GWAS Catalog, Diabetes care 2023, PMID:37308106. 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.
Type 2 diabetes (age of onset) (rs3011366). MyGeneLog™. https://www.mygenelog.com/variants/rs3011366