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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
The effect
Each copy of the C allele shifted the measure 0.224 mmol/l lower (95% confidence interval 0.18-0.27); p = 2 × 10−19.
How common The C allele had a frequency of about 25% in the people studied.
Where it sits Chromosome 8, band 8p21.3 — in an intron of LPL.
What each result means
A/ANo copy of the version the research linked to Postprandial small VLDL particle concentration. This is the starting point the study compared everyone against.
A/COne copy of the version the research linked to Postprandial small VLDL particle concentration. That is a smaller link than two copies.
C/CTwo copies of the version the research linked to Postprandial small VLDL particle concentration. That is the strongest link of the three results. A link in a study is not a diagnosis.
rs295 is a single position in the genome, in or near the LPL gene. Published research associates it with postprandial small vldl particle concentration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs295 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 rs295 come from?
GWAS Catalog, Diabetes 2021, PMID:34610981. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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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.
Postprandial small VLDL particle concentration (rs295). MyGeneLog™. https://www.mygenelog.com/variants/rs295