4 3512822317Reads by AI crawlersClaude1ChatGPT2Google · Gemini0Perplexity0Meta AI8Microsoft · Copilot2Amazon2Apple3Others17Total35Counted 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 25,662 British ancestry cases, 17,928 British ancestry controls; replicated in 13,367 European ancestry cases, 11,851 European ancestry controls, 3,436 cases, 2,435 controls.
The effect
Each copy of the C allele shifted the measure 0.21 lower (95% confidence interval 0.16-0.26); p = 5 × 10−17.
Where it sits Chromosome 1, band 1p36.11 — between genes, 2.4 kb from MIR4425.
What each result means
C/CPublished research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Male-pattern baldness compared to the general population.
C/TPublished research associates this genotype (one copy of the reported risk allele) with an intermediate association with Male-pattern baldness.
T/TPublished research associates this genotype with typical/baseline likelihood of Male-pattern baldness — no copies of the reported risk allele.
Nature communications · 2017 · PMID 29146897 · open access
Questions about rs11249243
What is rs11249243?
rs11249243 is a single position in the genome, in or near the SYF2 gene. Published research associates it with male-pattern baldness. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs11249243 linked to?
On MyGeneLog this position is linked to Androgenetic Alopecia (Male Pattern Baldness). The research behind each link, and its sources, are set out on that condition page.
Does having rs11249243 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 rs11249243 come from?
GWAS Catalog, Nat Commun 2017, PMID:29146897. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
4 3512822317Reads by AI crawlersClaude1ChatGPT2Google · Gemini0Perplexity0Meta AI8Microsoft · Copilot2Amazon2Apple3Others17Total35Counted 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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