1 24214122210Reads by AI crawlersClaude0ChatGPT2Google · Gemini0Perplexity1Meta AI4Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others10Total24Counted 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 424 Korean ancestry cases, 5,402 Korean ancestry controls.
The effect
Each copy of the T allele carried 2.67 times the odds of Nonalcoholic fatty liver disease (without comorbidities) (95% confidence interval 1.9-3.81); p = 2 × 10−8.
Where it sits Chromosome 13, band 13q32.1 — in an intron of CLDN10.
What each result means
A/ANo copy of the version the research linked to Nonalcoholic fatty liver disease (without comorbidities). This is the starting point the study compared everyone against.
A/TOne copy of the version the research linked to Nonalcoholic fatty liver disease (without comorbidities). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Nonalcoholic fatty liver disease (without comorbidities). That is the strongest link of the three results. A link in a study is not a diagnosis.
rs7996045 is a single position in the genome, in or near the CLDN10 gene. Published research associates it with nonalcoholic fatty liver disease (without comorbidities). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7996045 linked to?
On MyGeneLog this position is linked to Nonalcoholic Fatty Liver Disease (NAFLD). The research behind each link, and its sources, are set out on that condition page.
Does having rs7996045 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 rs7996045 come from?
GWAS Catalog, GWAS Catalog n.d., PMID:37133724. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
1 24214122210Reads by AI crawlersClaude0ChatGPT2Google · Gemini0Perplexity1Meta AI4Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others10Total24Counted 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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