0 312Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others2Total3Counted 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 829 European ancestry female cases, 2,591 European ancestry female controls.
The effect
Each copy of the A allele carried 2.95 times the odds of Venous thromboembolism recurrence in VTE (95% confidence interval 2.045845-4.252183); p = 7 × 10−9.
How common The A allele had a frequency of about 1% in the people studied.
Where it sits Chromosome 4, band 4q12 — between genes, 15.1 kb from SPMAP2L.
What each result means
A/ATwo copies of the version the research linked to Venous thromboembolism recurrence in VTE. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/TOne copy of the version the research linked to Venous thromboembolism recurrence in VTE. That is a smaller link than two copies.
T/TNo copy of the version the research linked to Venous thromboembolism recurrence in VTE. This is the starting point the study compared everyone against.
rs28752105 is a single position in the genome, in or near the near SPMAP2L gene. Published research associates it with venous thromboembolism recurrence in 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 rs28752105 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 rs28752105 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 rs28752105 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 312Reads by AI crawlersClaude1ChatGPT0Google · Gemini0Perplexity0Meta AI0Microsoft · Copilot0Amazon0Apple0China (ByteDance, Huawei, Baidu…)0Others2Total3Counted 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.
Venous thromboembolism recurrence in VTE (rs28752105). MyGeneLog™. https://www.mygenelog.com/variants/rs28752105