Standard

Cholesterol to total lipids ratio in very large VLDL

LINC00529 · rs10110008

What the study found

Who was studied 114,160 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0364 higher (95% confidence interval 0.029-0.044); p = 1 × 10−19.

How common The G allele had a frequency of about 42% in the people studied.

Where it sits Chromosome 8, band 8p23.1 — inside LINC00529.

What each result means

G/G Two copies of the version the research linked to Cholesterol to total lipids ratio in very large VLDL. That is the strongest link of the three results. A link in a study is not a diagnosis.
G/T One copy of the version the research linked to Cholesterol to total lipids ratio in very large VLDL. That is a smaller link than two copies.
T/T No copy of the version the research linked to Cholesterol to total lipids ratio in very large VLDL. This is the starting point the study compared everyone against.
Source

Questions about rs10110008

What is rs10110008?

rs10110008 is a single position in the genome, in or near the LINC00529 gene. Published research associates it with cholesterol to total lipids ratio in very large vldl. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs10110008 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 rs10110008 come from?

GWAS Catalog, PLoS biology 2022, PMID:35213538. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

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.

Cholesterol to total lipids ratio in very large VLDL (rs10110008). MyGeneLog™. https://www.mygenelog.com/variants/rs10110008

← See all variants