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Aspartate aminotransferase levels

ARNT · rs61817641

What the study found

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

The effect Each copy of the T allele shifted the measure 0.0251 higher (95% confidence interval 0.021-0.029); p = 2 × 10−35.

Where it sits Chromosome 1, band 1q21.3 — in an intron of ARNT.

What each result means

C/C No copy of the version the research linked to Aspartate aminotransferase levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to Aspartate aminotransferase levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to Aspartate aminotransferase levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs61817641

What is rs61817641?

rs61817641 is a single position in the genome, in or near the ARNT gene. Published research associates it with aspartate 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 rs61817641 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 rs61817641 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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Aspartate aminotransferase levels (rs61817641). MyGeneLog™. https://www.mygenelog.com/variants/rs61817641

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