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Who was studied 394,642 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.0148 lower (95% confidence interval 0.011-0.019); p = 1 × 10−12.
How common The C allele had a frequency of about 29% in the people studied.
Where it sits Chromosome 11, band 11p15.5 — between genes, 1.5 kb from KRTAP5-4.
What each result means
C/CTwo copies of the version the research linked to IGF 1 (UKB data field 30770). That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to IGF 1 (UKB data field 30770). That is a smaller link than two copies.
T/TNo copy of the version the research linked to IGF 1 (UKB data field 30770). This is the starting point the study compared everyone against.
Nature genetics · 2025 · PMID 39789286 · open access
Questions about rs11605284
What is rs11605284?
rs11605284 is a single position in the genome, in or near the near KRTAP5-4 gene. Published research associates it with igf 1 (ukb data field 30770). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs11605284 linked to?
On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs11605284 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 rs11605284 come from?
GWAS Catalog, Nature genetics 2025, PMID:39789286. 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.
IGF 1 (UKB data field 30770) (rs11605284). MyGeneLog™. https://www.mygenelog.com/variants/rs11605284