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Low density lipoprotein cholesterol levels

GCNT4 · rs9293641

What the study found

Who was studied 341,875 European ancestry individuals, 6,003 African ancestry individuals, 7,319 South Asian ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0405 higher (95% confidence interval 0.033-0.048); p = 3 × 10−24.

Where it sits Chromosome 5, band 5q13.3 — in an intron of GCNT4.

What each result means

A/A 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.
A/C One copy of the version the research linked to Low density lipoprotein cholesterol levels. That is a smaller link than two copies.
C/C 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 rs9293641

What is rs9293641?

rs9293641 is a single position in the genome, in or near the GCNT4 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 rs9293641 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 rs9293641 come from?

GWAS Catalog, Nature genetics 2021, PMID:33462484. 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.

Low density lipoprotein cholesterol levels (rs9293641). MyGeneLog™. https://www.mygenelog.com/variants/rs9293641

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