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Non-HDL cholesterol levels

LINC01301 · rs6992869

What the study found

Who was studied 1,320,016 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0129 lower (95% confidence interval 0.0096-0.0162); p = 9 × 10−11.

How common The T allele had a frequency of about 63% in the people studied.

Where it sits Chromosome 8, band 8q12.1 — in an intron of LINC01301.

What each result means

C/C No copy of the version the research linked to Non-HDL cholesterol levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Non-HDL cholesterol levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Non-HDL cholesterol levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs6992869

What is rs6992869?

rs6992869 is a single position in the genome, in or near the LINC01301 gene. Published research associates it with non-hdl cholesterol levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs6992869 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 rs6992869 come from?

GWAS Catalog, Nature 2021, PMID:34887591. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.

Quoting this page

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Non-HDL cholesterol levels (rs6992869). MyGeneLog™. https://www.mygenelog.com/variants/rs6992869

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