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Phospholipid levels in chylomicrons and extremely large VLDL

SPRING1 · rs11832734

Where this position leads

Condition: Cholesterol (LDL, HDL and Total)

rs11832734 Condition: Cholesterol (LDL, HDL and Total) Cholesterol (LDL, HDL and Total) Condition rs11832734 rs11832734 SPRING1

What the study found

Who was studied 434,646 British ancestry individuals, 8,796 British Central/South Asian individuals, 6,573 British African individuals.

The effect Each copy of the A allele shifted the measure 0.02 mmol/L lower (95% confidence interval 0.02-0.02); p = 1 × 10−13.

Where it sits Chromosome 12, band 12q24.22 — in the 5′ untranslated region of SPRING1.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Phospholipid levels in chylomicrons and extremely large VLDL compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with Phospholipid levels in chylomicrons and extremely large VLDL.
G/G Published research associates this genotype with typical/baseline likelihood of Phospholipid levels in chylomicrons and extremely large VLDL — no copies of the reported risk allele.
Source

Questions about rs11832734

What is rs11832734?

rs11832734 is a single position in the genome, in or near the SPRING1 gene. Published research associates it with phospholipid levels in chylomicrons and extremely large vldl. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs11832734 linked to?

On MyGeneLog this position is linked to Cholesterol (LDL, HDL and Total). The research behind each link, and its sources, are set out on that condition page.

Does having rs11832734 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 rs11832734 come from?

GWAS Catalog, Nature genetics 2025, PMID:41044249. 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.

Phospholipid levels in chylomicrons and extremely large VLDL (rs11832734). MyGeneLog™. https://www.mygenelog.com/variants/rs11832734

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