Urine S(2-carboxyethyl)mercapturic acid levels in chronic kidney disease
near SRP14P4 · rs10912836
0 523Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others3Total5Counted 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 3,647 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.349 lower (95% confidence interval 0.29-0.41); p = 7 × 10−32.
How common The C allele had a frequency of about 32% in the people studied.
Where it sits Chromosome 1, band 1q24.3 — between genes, 16.3 kb from SRP14P4.
What each result means
C/CTwo copies of the version the research linked to Urine S(2-carboxyethyl)mercapturic acid levels in chronic kidney disease. 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 Urine S(2-carboxyethyl)mercapturic acid levels in chronic kidney disease. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Urine S(2-carboxyethyl)mercapturic acid levels in chronic kidney disease. This is the starting point the study compared everyone against.
Nature genetics · 2023 · PMID 37277652 · open access
Questions about rs10912836
What is rs10912836?
rs10912836 is a single position in the genome, in or near the near SRP14P4 gene. Published research associates it with urine s(2-carboxyethyl)mercapturic acid levels in chronic kidney disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs10912836 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 rs10912836 come from?
GWAS Catalog, Nature genetics 2023, PMID:37277652. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 523Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others3Total5Counted 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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