Familial combined hyperlipidemia defined by Consensus criteria
PLTP · rs6073952
0 16142216Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI4Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others6Total16Counted 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 G allele shifted the measure 0.0738 lower (95% confidence interval 0.055-0.093); p = 2 × 10−14.
How common The G allele had a frequency of about 81% in the people studied.
Where it sits Chromosome 20, band 20q13.12 — in an intron of PLTP.
What each result means
A/ANo 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.
A/GOne copy of the version the research linked to Familial combined hyperlipidemia defined by Consensus criteria. That is a smaller link than two copies.
G/GTwo 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.
rs6073952 is a single position in the genome, in or near the PLTP 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 rs6073952 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 rs6073952 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 rs6073952 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 16142216Reads by AI crawlersClaude0ChatGPT0Google · Gemini0Perplexity1Meta AI4Microsoft · Copilot0Amazon2Apple2China (ByteDance, Huawei, Baidu…)1ByteDance (Doubao)1Others6Total16Counted 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 (rs6073952). MyGeneLog™. https://www.mygenelog.com/variants/rs6073952