0 251223116Reads by AI crawlersClaude1ChatGPT2Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others16Total25Counted 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.
Who was studied 342,376 European ancestry individuals, 6,016 African ancestry individuals, 7,339 South Asian ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.0669 higher (95% confidence interval 0.05-0.084); p = 4 × 10−15.
Where it sits Chromosome 15, band 15q24.3 — between genes, 0.8 kb from RCN2.
What each result means
C/CNo copy of the version the research linked to Creatinine levels. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Creatinine levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Creatinine levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature genetics · 2021 · PMID 33462484 · open access
Questions about rs932046
What is rs932046?
rs932046 is a single position in the genome, in or near the near RCN2 gene. Published research associates it with creatinine levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs932046 linked to?
On MyGeneLog this position is linked to Kidney Function, Gout. The research behind each link, and its sources, are set out on that condition page.
Does having rs932046 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 rs932046 come from?
GWAS Catalog, Nature genetics 2021, PMID:33462484. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 251223116Reads by AI crawlersClaude1ChatGPT2Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others16Total25Counted 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.
Quoting this page
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.