Branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid levels
ACOT2 · rs113425878
0 422Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total4Counted 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 8,256 European ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.234 lower (95% confidence interval 0.17-0.3); p = 2 × 10−12.
How common The G allele had a frequency of about 5% in the people studied.
Where it sits Chromosome 14, band 14q24.3 — in an intron of ACOT2.
What each result means
C/CNo copy of the version the research linked to Branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid levels. This is the starting point the study compared everyone against.
C/GOne copy of the version the research linked to Branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid levels. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs113425878 is a single position in the genome, in or near the ACOT2 gene. Published research associates it with branched-chain, straight-chain, or cyclopropyl 12:1 fatty acid levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs113425878 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 rs113425878 come from?
GWAS Catalog, Nature genetics 2023, PMID:36635386. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 422Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total4Counted 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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