Venous thromboembolism recurrence in deep vein thrombosis as first VTE
near RNA5SP441 · rs117366080
0 6114Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon1Apple0China (ByteDance, Huawei, Baidu…)0Others4Total6Counted 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 1,074 European ancestry cases, 2,325 European ancestry controls.
The effect
Each copy of the A allele carried 2.82 times the odds of Venous thromboembolism recurrence in deep vein thrombosis as first VTE (95% confidence interval 1.989194-3.9946); p = 6 × 10−9.
How common The A allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 17, band 17q21.2 — between genes, 5.1 kb from RNA5SP441.
What each result means
A/ATwo copies of the version the research linked to Venous thromboembolism recurrence in deep vein thrombosis as first VTE. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Venous thromboembolism recurrence in deep vein thrombosis as first VTE. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Venous thromboembolism recurrence in deep vein thrombosis as first VTE. This is the starting point the study compared everyone against.
rs117366080 is a single position in the genome, in or near the near RNA5SP441 gene. Published research associates it with venous thromboembolism recurrence in deep vein thrombosis as first vte. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs117366080 linked to?
On MyGeneLog this position is linked to Venous Thromboembolism. The research behind each link, and its sources, are set out on that condition page.
Does having rs117366080 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 rs117366080 come from?
GWAS Catalog, Blood 2025, PMID:40811855. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 6114Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon1Apple0China (ByteDance, Huawei, Baidu…)0Others4Total6Counted 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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Venous thromboembolism recurrence in deep vein thrombosis as first VTE (rs117366080). MyGeneLog™. https://www.mygenelog.com/variants/rs117366080