Familial combined hyperlipidemia defined by Consensus criteria
ATXN7L2 · rs41279732
0 16132217Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI3Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others7Total16Counted 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 0.131 higher (95% confidence interval 0.099-0.163); p = 4 × 10−16.
How common The T allele had a frequency of about 93% in the people studied.
Where it sits Chromosome 1, band 1p13.3 — in an intron of ATXN7L2.
What each result means
G/GNo 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.
G/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.
rs41279732 is a single position in the genome, in or near the ATXN7L2 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 rs41279732 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 rs41279732 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 rs41279732 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 16132217Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI3Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others7Total16Counted 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 (rs41279732). MyGeneLog™. https://www.mygenelog.com/variants/rs41279732