Venous thromboembolism adjusted for sickle cell variant rs77121243-T
LEMD3 · rs138916004
0 394723320Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity4Meta AI7Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)3ByteDance (Doubao)3Others20Total39Counted 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 393 African American cases, 4,941 African American controls..
The effect
Each copy of the G allele carried 3.17 times the odds of Venous thromboembolism adjusted for sickle cell variant rs77121243-T (95% confidence interval 2.131-4.719); p = 1 × 10−8.
How common The G allele had a frequency of about 2% in the people studied.
Where it sits Chromosome 12, band 12q14.3 — in an intron of LEMD3.
What each result means
A/ANo copy of the version the research linked to Venous thromboembolism adjusted for sickle cell variant rs77121243-T. This is the starting point the study compared everyone against.
A/GOne copy of the version the research linked to Venous thromboembolism adjusted for sickle cell variant rs77121243-T. That is a smaller link than two copies.
G/GTwo copies of the version the research linked to Venous thromboembolism adjusted for sickle cell variant rs77121243-T. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs138916004 is a single position in the genome, in or near the LEMD3 gene. Published research associates it with venous thromboembolism adjusted for sickle cell variant rs77121243-t. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs138916004 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 rs138916004 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 rs138916004 come from?
GWAS Catalog, Thromb Haemost 2017, PMID:28203683. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 394723320Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity4Meta AI7Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)3ByteDance (Doubao)3Others20Total39Counted 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.