1 402229124216Reads by AI crawlersClaude0ChatGPT2Google · Gemini2Perplexity2Meta AI9Microsoft · Copilot1Amazon2Apple4China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others16Total40Counted 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 0.285 higher (95% confidence interval 0.24-0.32); p = 5 × 10−45.
Where it sits Chromosome 20, band 20p11.22 — between genes, 141.2 kb from LINC01432.
What each result means
C/CTwo copies of the version the research linked to Male-pattern baldness. That is the strongest link of the three results. A link in a study is not a diagnosis.
C/TOne copy of the version the research linked to Male-pattern baldness. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Male-pattern baldness. This is the starting point the study compared everyone against.
Nature communications · 2017 · PMID 29146897 · open access
Questions about rs77410716
What is rs77410716?
rs77410716 is a single position in the genome, in or near the PAX1 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 rs77410716 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 rs77410716 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 rs77410716 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.
1 402229124216Reads by AI crawlersClaude0ChatGPT2Google · Gemini2Perplexity2Meta AI9Microsoft · Copilot1Amazon2Apple4China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others16Total40Counted 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
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.