Proprotein convertase subtilisin/kexin type 7 levels
near PAFAH1B2 · rs9326248
0 927Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others7Total9Counted 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 997 European ancestry individuals; replicated in 338 Greater Middle Eastern (Middle Eastern, North African or Persian), South Asian ancestry, Asian ancestry individuals.
The effect
Each copy of the T allele shifted the measure 0.993 lower (95% confidence interval 0.91-1.07); p = 2 × 10−105.
Where it sits Chromosome 11, band 11q23.3 — between genes, 15.8 kb from PAFAH1B2.
What each result means
G/GNo copy of the version the research linked to Proprotein convertase subtilisin/kexin type 7 levels. This is the starting point the study compared everyone against.
G/TOne copy of the version the research linked to Proprotein convertase subtilisin/kexin type 7 levels. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Proprotein convertase subtilisin/kexin type 7 levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Nature communications · 2017 · PMID 28240269 · open access
Questions about rs9326248
What is rs9326248?
rs9326248 is a single position in the genome, in or near the near PAFAH1B2 gene. Published research associates it with proprotein convertase subtilisin/kexin type 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 rs9326248 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 rs9326248 come from?
GWAS Catalog, Nature communications 2017, PMID:28240269. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 927Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others7Total9Counted 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
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Proprotein convertase subtilisin/kexin type 7 levels (rs9326248). MyGeneLog™. https://www.mygenelog.com/variants/rs9326248