0 3813129123214Reads by AI crawlersClaude1ChatGPT3Google · Gemini1Perplexity2Meta AI9Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others14Total38Counted 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 73,265 European ancestry individuals.
The effect
Each copy of the C allele shifted the measure 0.175 lower (95% confidence interval 0.12-0.23); p = 4 × 10−9.
Where it sits Chromosome 14, band 14q31.1 — between genes, 55.7 kb from LOC105370590.
What each result means
A/ANo copy of the version the research linked to Rosacea symptom severity. This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Rosacea symptom severity. That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Rosacea symptom severity. That is the strongest link of the three results. A link in a study is not a diagnosis.
Human molecular genetics · 2018 · PMID 29771307 · open access
Questions about rs149851565
What is rs149851565?
rs149851565 is a single position in the genome, in or near the NRXN3 gene. Published research associates it with rosacea symptom severity. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs149851565 linked to?
On MyGeneLog this position is linked to Rosacea. The research behind each link, and its sources, are set out on that condition page.
Does having rs149851565 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 rs149851565 come from?
GWAS Catalog, Hum Mol Genet 2018, PMID:29771307. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 3813129123214Reads by AI crawlersClaude1ChatGPT3Google · Gemini1Perplexity2Meta AI9Microsoft · Copilot1Amazon2Apple3China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others14Total38Counted 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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