Coronary artery disease and LDL cholesterol levels (multivariate analysis)
near BNC2 · rs7033354
0 232161319Reads by AI crawlersClaude0ChatGPT2Google · Gemini0Perplexity1Meta AI6Microsoft · Copilot0Amazon1Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others9Total23Counted 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 122,733 coronary artery disease cases, 424,528 coronary artery disease controls, 188,577 individuals.
The effect
The reported allele is T; the catalogue records no effect size
; p = 1 × 10−8.
How common The T allele had a frequency of about 63% in the people studied.
Where it sits Chromosome 9, band 9p22.2 — between genes, 33.9 kb from BNC2.
What each result means
C/CNo copy of the version the research linked to Coronary artery disease and LDL cholesterol levels (multivariate analysis). This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Coronary artery disease and LDL cholesterol levels (multivariate analysis). That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Coronary artery disease and LDL cholesterol levels (multivariate analysis). That is the strongest link of the three results. A link in a study is not a diagnosis.
Circulation. Genomic and precision medicine · 2018 · PMID 30525989
Questions about rs7033354
What is rs7033354?
rs7033354 is a single position in the genome, in or near the near BNC2 gene. Published research associates it with coronary artery disease and ldl cholesterol levels (multivariate analysis). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs7033354 linked to?
On MyGeneLog this position is linked to Coronary Artery Disease. The research behind each link, and its sources, are set out on that condition page.
Does having rs7033354 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 rs7033354 come from?
GWAS Catalog, Circ Genom Precis Med 2018, PMID:30525989. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 232161319Reads by AI crawlersClaude0ChatGPT2Google · Gemini0Perplexity1Meta AI6Microsoft · Copilot0Amazon1Apple3China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others9Total23Counted 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.