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Triglyceride levels

CEP164 · rs11216358

What the study found

Who was studied 48,057 Hispanic individuals.

The effect Each copy of the A allele shifted the measure 0.206 higher (95% confidence interval 0.17-0.24); p = 6 × 10−33.

How common The A allele had a frequency of about 6% in the people studied.

Where it sits Chromosome 11, band 11q23.3 — in an intron of CEP164.

What each result means

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

Questions about rs11216358

What is rs11216358?

rs11216358 is a single position in the genome, in or near the CEP164 gene. Published research associates it with triglyceride levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs11216358 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 rs11216358 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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Triglyceride levels (rs11216358). MyGeneLog™. https://www.mygenelog.com/variants/rs11216358

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