Cognitive decline rate in late mild cognitive impairment
GNAI1 · rs799979
0 3132313222112Reads by AI crawlersClaude3ChatGPT2Google · Gemini3Perplexity1Meta AI3Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others12Total31Counted 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 472 European ancestry cases, 47 cases.
The effect
Each copy of the A allele shifted the measure 0.578 higher (95% confidence interval 0.35-0.81); p = 1 × 10−6.
How common The A allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 7, band 7q21.11 — inside CD36.
What each result means
A/ATwo copies of the version the research linked to Cognitive decline rate in late mild cognitive impairment. 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 Cognitive decline rate in late mild cognitive impairment. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Cognitive decline rate in late mild cognitive impairment. This is the starting point the study compared everyone against.
rs799979 is a single position in the genome, in or near the GNAI1 gene. Published research associates it with cognitive decline rate in late mild cognitive impairment. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs799979 linked to?
On MyGeneLog this position is linked to Cognitive Decline Rate in Late MCI. The research behind each link, and its sources, are set out on that condition page.
Does having rs799979 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 rs799979 come from?
GWAS Catalog, PLoS One 2015, PMID:26252872. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 3132313222112Reads by AI crawlersClaude3ChatGPT2Google · Gemini3Perplexity1Meta AI3Microsoft · Copilot2Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others12Total31Counted 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.
Cognitive decline rate in late mild cognitive impairment (rs799979). MyGeneLog™. https://www.mygenelog.com/variants/rs799979