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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 12,328 European ancestry males, 15,813 European ancestry females.
The effect
Each copy of the T allele shifted the measure 0.05 mg/dl higher (95% confidence interval 0.035-0.068); p = 1 × 10−9.
How common The T allele had a frequency of about 42% in the people studied.
Where it sits Chromosome 2, band 2p23.3 — in an intron of GCKR.
What each result means
C/CNo copy of the version the research linked to Uric acid levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Uric acid levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Uric acid levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs780094
What is rs780094?
rs780094 is a single position in the genome, in or near the GCKR gene. Published research associates it with uric acid levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What do people read about alongside rs780094?
Subjects that appear in the title or abstract of the same papers as this rsID include blood sugar and insulin (64 papers), cholesterol and blood fats (10 papers), heart and circulation (6 papers), alcohol and the flush (5 papers), liver (5 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs780094 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 rs780094 come from?
GWAS Catalog, PLoS Genet 2009, PMID:19503597. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
7 6042366221430Reads by AI crawlersClaude4ChatGPT2Google · Gemini3Perplexity6Meta AI6Microsoft · Copilot2Amazon2Apple1China (ByteDance, Huawei, Baidu…)4ByteDance (Doubao)4Others30Total60Counted 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.
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