0 1512228Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others8Total15Counted 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 3,657 Sardinian (founder/genetic isolate) ancestry individuals.
The effect
Each copy of the T allele shifted the measure 1.52 lower (95% confidence interval 1.45-1.58).
How common The T allele had a frequency of about 10% in the people studied.
Where it sits Chromosome 22, band 22q13.2 — between genes, 2.7 kb from TNFRSF13C.
What each result means
C/CNo copy of the version the research linked to BAFF-R on IgD+ CD38dim B cell. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to BAFF-R on IgD+ CD38dim B cell. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to BAFF-R on IgD+ CD38dim B cell. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs73165129 is a single position in the genome, in or near the near TNFRSF13C gene. Published research associates it with baff-r on igd+ cd38dim b cell. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs73165129 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 rs73165129 come from?
GWAS Catalog, GWAS Catalog n.d., PMID:32929287. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 1512228Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others8Total15Counted 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.
BAFF-R on IgD+ CD38dim B cell (rs73165129). MyGeneLog™. https://www.mygenelog.com/variants/rs73165129