5 543258122229Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity5Meta AI8Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others29Total54Counted 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.
Solid lines are connections this site curates. Dashed lines mean the two ends share a research paper — worth knowing, and not a claim that one explains the other.
What the study found
Who was studied 390 European ancestry cases, 364 European ancestry controls; replicated in 4,364 East Asian ancestry cases, 24,174 European ancestry controls, 3,564 East Asian ancestry controls, 24,391 European ancestry controls.
The effect
Each copy of the C allele carried 1.07 times the odds of Breast cancer (95% confidence interval 1.04-1.11); p = 3 × 10−9.
How common The C allele had a frequency of about 30% in the people studied.
Where it sits Chromosome 11, band 11p15.5 — in the 3′ untranslated region of LSP1.
What each result means
C/CTwo copies of the version the research linked to Breast cancer. 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 Breast cancer. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Breast cancer. This is the starting point the study compared everyone against.
Papers in Europe PMC whose title or abstract names both this rsID and that subject. A shared paper means somebody wrote about the two together — it is not a claim that this position explains the subject.
Questions about rs3817198
What is rs3817198?
rs3817198 is a single position in the genome, in or near the LSP1 gene. Published research associates it with breast cancer. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs3817198 linked to?
On MyGeneLog this position is linked to Breast Cancer. The research behind each link, and its sources, are set out on that condition page.
What do people read about alongside rs3817198?
Subjects that appear in the title or abstract of the same papers as this rsID include alcohol and the flush (4 papers), menopause (4 papers), fertility (3 papers), exercise and muscle (1 papers). A shared paper means somebody wrote about the two together; it is not a claim that this position explains the topic.
Does having rs3817198 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 rs3817198 come from?
GWAS Catalog, Nature 2007, PMID:17529967. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
5 543258122229Reads by AI crawlersClaude3ChatGPT2Google · Gemini0Perplexity5Meta AI8Microsoft · Copilot1Amazon2Apple2China (ByteDance, Huawei, Baidu…)2ByteDance (Doubao)2Others29Total54Counted 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.
Breast cancer (rs3817198). MyGeneLog™. https://www.mygenelog.com/variants/rs3817198