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High density lipoprotein cholesterol levels

near KLF14 · rs6974288

What the study found

Who was studied 62,138 Hispanic or Latino individuals.

The effect Each copy of the A allele shifted the measure 0.0366 lower (95% confidence interval 0.017-0.056); p = 1 × 10−12.

How common The A allele had a frequency of about 62% in the people studied.

Where it sits Chromosome 7, band 7q32.2 — between genes, 5.2 kb from KLF14.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of High density lipoprotein cholesterol levels compared to the general population.
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with High density lipoprotein cholesterol levels.
G/G Published research associates this genotype with typical/baseline likelihood of High density lipoprotein cholesterol levels — no copies of the reported risk allele.
Source

Questions about rs6974288

What is rs6974288?

rs6974288 is a single position in the genome, in or near the near KLF14 gene. Published research associates it with high 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 rs6974288 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 rs6974288 come from?

GWAS Catalog, Nature communications 2025, PMID:40210677. 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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High density lipoprotein cholesterol levels (rs6974288). MyGeneLog™. https://www.mygenelog.com/variants/rs6974288

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