Treatment or medication use - insulin product (UKB data field 20003_1140883066)
near MUC22 · rs115730672
0 312Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon1Apple0China (ByteDance, Huawei, Baidu…)0Others2Total3Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
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 4,469 European ancestry cases, 451,807 European ancestry controls.
The effect
Each copy of the C allele shifted the measure 1.05 higher (95% confidence interval 0.74-1.36); p = 3 × 10−11.
How common The C allele had a frequency of about 1% in the people studied.
Where it sits Chromosome 6, band 6p21.33 — between genes, 3.9 kb from MUC22.
What each result means
C/CTwo copies of the version the research linked to Treatment or medication use - insulin product (UKB data field 20003_1140883066). 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 Treatment or medication use - insulin product (UKB data field 20003_1140883066). That is a smaller link than two copies.
T/TNo copy of the version the research linked to Treatment or medication use - insulin product (UKB data field 20003_1140883066). This is the starting point the study compared everyone against.
rs115730672 is a single position in the genome, in or near the near MUC22 gene. Published research associates it with treatment or medication use - insulin product (ukb data field 20003_1140883066). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs115730672 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 rs115730672 come from?
GWAS Catalog, Nature genetics 2021, PMID:34737426. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 312Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon1Apple0China (ByteDance, Huawei, Baidu…)0Others2Total3Counted by the name each crawler declares; requests found to be impersonating one are left out. Google · Gemini includes Googlebot, the search crawler whose index Google also uses for its AI features. Other search engines and bots are under Others.
Quoting this page
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Treatment or medication use - insulin product (UKB data field 20003_1140883066) (rs115730672). MyGeneLog™. https://www.mygenelog.com/variants/rs115730672