0 332223622329Reads by AI crawlersClaude2ChatGPT2Google · Gemini2Perplexity3Meta AI6Microsoft · Copilot2Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others9Total33Counted 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 up to 15,007 European ancestry male individuals, up to 16,943 European ancestry female individuals.
The effect
Each copy of the G allele shifted the measure 0.0168 lower (95% confidence interval 0.0098-0.0237); p = 2 × 10−6.
How common The G allele had a frequency of about 88% in the people studied.
Where it sits Chromosome 17, band 17q25.3 — in an intron of RBFOX3.
What each result means
A/ANo copy of the version the research linked to Urate levels (BMI interaction). This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Urate levels (BMI interaction). That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Urate levels (BMI interaction). That is the strongest link of the three results. A link in a study is not a diagnosis.
rs898534 is a single position in the genome, in or near the RBFOX3 gene. Published research associates it with urate levels (bmi interaction). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs898534 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 rs898534 come from?
GWAS Catalog, PLoS One 2015, PMID:25811787. 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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