Standard

Alanine aminotransferase levels

LINC02288 · rs75004998

Stands on its own. Nothing else here links to this position yet — but the page above is the point: what the research found, what each genotype means, and where it came from, in language you can read. Links to conditions, drugs and the senses appear automatically if we write them.

What the study found

Who was studied 507,850 East Asian ancestry individuals, 420,829 European ancestry individuals.

The effect Each copy of the A allele shifted the measure 0.0095 lower (95% confidence interval 0.0066-0.0124); p = 3 × 10⁻¹⁰.

Where it sits Chromosome 14, band 14q24.3 — in an intron of LINC02288.

What each result means

A/A Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of Alanine aminotransferase 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 Alanine aminotransferase levels.

G/G Published research associates this genotype with typical/baseline likelihood of Alanine aminotransferase levels — no copies of the reported risk allele.

Source

Genome-wide association studies in a large Korean cohort identify quantitative trait loci for 36 traits and illuminate their genetic architectures

Jee YH, Wang Y, Jung KJ, Lee JY, Kimm H, Duan R, Price AL, Martin AR, Kraft P

Nature communications · 2025 · PMID 40436827 · open access

Questions about rs75004998

What is rs75004998?

rs75004998 is a single position in the genome, in or near the LINC02288 gene. Published research associates it with alanine aminotransferase levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs75004998 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 rs75004998 come from?

GWAS Catalog, Nature communications 2025, PMID:40436827. 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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Alanine aminotransferase levels (rs75004998). MyGeneLog™. https://www.mygenelog.com/variants/rs75004998

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