1 121227Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others7Total12Counted 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 3,506 European ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.987 higher (95% confidence interval 0.95-1.02).
How common The T allele had a frequency of about 29% in the people studied.
Where it sits Chromosome 19, band 19q13.41 — in the 3′ untranslated region of SIGLEC9.
What each result means
G/GNo copy of the version the research linked to Sialic acid-binding Ig-like lectin 7 levels. This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Sialic acid-binding Ig-like lectin 7 levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Sialic acid-binding Ig-like lectin 7 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs12983058 is a single position in the genome, in or near the SIGLEC9 gene. Published research associates it with sialic acid-binding ig-like lectin 7 levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs12983058 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 rs12983058 come from?
GWAS Catalog, Nature genetics 2024, PMID:39528825. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
1 121227Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)0Others7Total12Counted 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.