Alzheimer's disease or educational attainment (pleiotropy)
BSN · rs7614725
2 25623113Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot6Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others13Total25Counted 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 (see Lambert 2013 and Okbay 2016).
The effect
Each copy of the A allele shifted the measure 98.9 z score higher; p = 2 × 10−20.
How common The A allele had a frequency of about 30% in the people studied.
Where it sits Chromosome 3, band 3p21.31 — in an intron of BSN.
What each result means
A/ATwo copies of the version the research linked to Alzheimer's disease or educational attainment (pleiotropy). That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Alzheimer's disease or educational attainment (pleiotropy). That is a smaller link than two copies.
G/GNo copy of the version the research linked to Alzheimer's disease or educational attainment (pleiotropy). This is the starting point the study compared everyone against.
rs7614725 is a single position in the genome, in or near the BSN gene. Published research associates it with alzheimer's disease or educational attainment (pleiotropy). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7614725 linked to?
On MyGeneLog this position is linked to Alzheimer's Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs7614725 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 rs7614725 come from?
GWAS Catalog, GeroScience 2022, PMID:34743297. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
2 25623113Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot6Amazon2Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others13Total25Counted 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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Alzheimer's disease or educational attainment (pleiotropy) (rs7614725). MyGeneLog™. https://www.mygenelog.com/variants/rs7614725