Proprotein convertase subtilisin/kexin type 7 levels
PAFAH1B2 · rs144600500
0 422Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total4Counted 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 2,935 Qatari ancestry individuals.
The effect
Each copy of the G allele shifted the measure 0.675 lower (95% confidence interval 0.48-0.87); p = 1 × 10−11.
How common The G allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 11, band 11q23.3 — in an intron of PAFAH1B2.
What each result means
A/ANo 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.
A/GOne copy of the version the research linked to Proprotein convertase subtilisin/kexin type 7 levels. That is a smaller link than two copies.
G/GTwo 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.
Human molecular genetics · 2023 · PMID 36168886 · open access
Questions about rs144600500
What is rs144600500?
rs144600500 is a single position in the genome, in or near the 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 rs144600500 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 rs144600500 come from?
GWAS Catalog, Human molecular genetics 2023, PMID:36168886. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 422Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others2Total4Counted 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 (rs144600500). MyGeneLog™. https://www.mygenelog.com/variants/rs144600500