Sensitive

Metabolic syndrome

LPL · rs249

What the study found

Who was studied 24,171 Taiwanese ancestry cases, 83,059 Taiwanese ancestry controls.

The effect Each copy of the T allele shifted the measure 0.215 lower (95% confidence interval 0.17-0.26); p = 4 × 10−20.

How common The T allele had a frequency of about 5% in the people studied.

Where it sits Chromosome 8, band 8p21.3 — in an intron of LPL.

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of Metabolic syndrome — no copies of the reported risk allele.
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Metabolic syndrome.
T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Metabolic syndrome compared to the general population.
Source

Questions about rs249

What is rs249?

rs249 is a single position in the genome, in or near the LPL gene. Published research associates it with metabolic syndrome. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs249 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 rs249 come from?

GWAS Catalog, Nutrients 2023, PMID:38201907. 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.

Metabolic syndrome (rs249). MyGeneLog™. https://www.mygenelog.com/variants/rs249

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