Low affinity immunoglobulin gamma Fc region receptor II-b levels
NOS1AP · rs189676321
0 11128Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others8Total11Counted 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 2,935 Qatari ancestry individuals.
The effect
Each copy of the A allele shifted the measure 0.481 higher (95% confidence interval 0.37-0.59); p = 1 × 10−18.
How common The A allele had a frequency of about 6% in the people studied.
Where it sits Chromosome 1, band 1q23.3 — in an intron of NOS1AP.
What each result means
A/ATwo copies of the version the research linked to Low affinity immunoglobulin gamma Fc region receptor II-b levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Low affinity immunoglobulin gamma Fc region receptor II-b levels. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Low affinity immunoglobulin gamma Fc region receptor II-b levels. This is the starting point the study compared everyone against.
Human molecular genetics · 2023 · PMID 36168886 · open access
Questions about rs189676321
What is rs189676321?
rs189676321 is a single position in the genome, in or near the NOS1AP gene. Published research associates it with low affinity immunoglobulin gamma fc region receptor ii-b levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does rs189676321 affect how medicines work?
NOS1AP carries pharmacogenomic findings for QT-prolonging medicines. That is educational information, not a prescription or a dosing guide. Any decision to start, stop or change a medicine belongs with the clinician or pharmacist managing your treatment.
Does having rs189676321 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 rs189676321 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 11128Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon2Apple0China (ByteDance, Huawei, Baidu…)0Others8Total11Counted 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.
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Low affinity immunoglobulin gamma Fc region receptor II-b levels (rs189676321). MyGeneLog™. https://www.mygenelog.com/variants/rs189676321