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Total lipids in very small VLDL

TMPRSS11E · rs1117816

What the study found

Who was studied 4,435 East Asian ancestry individuals, 11,340 South Asian ancestry individuals, 120,241 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0372 lower (95% confidence interval 0.027-0.047); p = 8 × 10−14.

How common The A allele had a frequency of about 76% in the people studied.

Where it sits Chromosome 4, band 4q13.2 — in an intron of TMPRSS11E.

What each result means

A/A Two copies of the version the research linked to Total lipids in very small VLDL. 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 Total lipids in very small VLDL. That is a smaller link than two copies.
C/C No copy of the version the research linked to Total lipids in very small VLDL. This is the starting point the study compared everyone against.
Source

Questions about rs1117816

What is rs1117816?

rs1117816 is a single position in the genome, in or near the TMPRSS11E gene. Published research associates it with total lipids in very small vldl. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1117816 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 rs1117816 come from?

GWAS Catalog, Nature 2024, PMID:38448586. 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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Total lipids in very small VLDL (rs1117816). MyGeneLog™. https://www.mygenelog.com/variants/rs1117816

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