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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 A allele shifted the measure 0.05 mg/dl higher (95% confidence interval 0.036-0.072); p = 9 × 10−9.
How common The A allele had a frequency of about 70% in the people studied.
Where it sits Chromosome 6, band 6p22.2 — in an intron of CARMIL1.
What each result means
A/ATwo 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.
A/GOne copy of the version the research linked to Uric acid levels. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Uric acid levels. This is the starting point the study compared everyone against.
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 rs742132
What is rs742132?
rs742132 is a single position in the genome, in or near the SCGN 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 rs742132?
Subjects that appear in the title or abstract of the same papers as this rsID include blood sugar and insulin (1 papers), heart and circulation (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs742132 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 rs742132 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.
6 5562244222229Reads by AI crawlersClaude6ChatGPT2Google · Gemini2Perplexity4Meta AI4Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others29Total55Counted 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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