0 101225Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others5Total10Counted 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 38,336 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.151 SD units higher (95% confidence interval 0.12-0.18); p = 6 × 10−24.
How common The T allele had a frequency of about 6% in the people studied.
Where it sits Chromosome 7, band 7p21.3 — in an intron of GLCCI1.
What each result means
C/CNo copy of the version the research linked to Neutrophil side fluorescence. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Neutrophil side fluorescence. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Neutrophil side fluorescence. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2023 · PMID 37596262 · open access
Questions about rs111677347
What is rs111677347?
rs111677347 is a single position in the genome, in or near the GLCCI1 gene. Published research associates it with neutrophil side fluorescence. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs111677347 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 rs111677347 come from?
GWAS Catalog, Nature communications 2023, PMID:37596262. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 101225Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others5Total10Counted 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.
Neutrophil side fluorescence (rs111677347). MyGeneLog™. https://www.mygenelog.com/variants/rs111677347