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Low density lipoprotein cholesterol levels

KPNB1-DT · rs12603290

What the study found

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

The effect Each copy of the C allele shifted the measure 0.0268 lower (95% confidence interval 0.024-0.03); p = 3 × 10−58.

How common The C allele had a frequency of about 51% in the people studied.

Where it sits Chromosome 17, band 17q21.32 — in an intron of KPNB1-DT.

What each result means

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

Questions about rs12603290

What is rs12603290?

rs12603290 is a single position in the genome, in or near the KPNB1-DT gene. Published research associates it with low density lipoprotein 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 rs12603290 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 rs12603290 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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Low density lipoprotein cholesterol levels (rs12603290). MyGeneLog™. https://www.mygenelog.com/variants/rs12603290

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