Familial combined hyperlipidemia defined by Consensus criteria
BABAM2 · rs55807911
0 1814238Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI4Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others8Total18Counted 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 39,961 British ancestry cases, 309,261 British ancestry controls.
The effect
Each copy of the T allele shifted the measure 0.0717 lower (95% confidence interval 0.052-0.091); p = 8 × 10−13.
How common The T allele had a frequency of about 80% in the people studied.
Where it sits Chromosome 2, band 2p23.2 — in an intron of BABAM2.
What each result means
C/CNo copy of the version the research linked to Familial combined hyperlipidemia defined by Consensus criteria. This is the starting point the study compared everyone against.
C/TOne copy of the version the research linked to Familial combined hyperlipidemia defined by Consensus criteria. That is a smaller link than two copies.
T/TTwo copies of the version the research linked to Familial combined hyperlipidemia defined by Consensus criteria. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs55807911 is a single position in the genome, in or near the BABAM2 gene. Published research associates it with familial combined hyperlipidemia defined by consensus criteria. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
What conditions is rs55807911 linked to?
On MyGeneLog this position is linked to Familial Combined Hyperlipidemia Defined by Consensus Criteria. The research behind each link, and its sources, are set out on that condition page.
Does having rs55807911 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 rs55807911 come from?
GWAS Catalog, Atherosclerosis 2022, PMID:34906840. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
0 1814238Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI4Microsoft · Copilot0Amazon2Apple3China (ByteDance, Huawei, Baidu…)0Others8Total18Counted 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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Familial combined hyperlipidemia defined by Consensus criteria (rs55807911). MyGeneLog™. https://www.mygenelog.com/variants/rs55807911