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Alanine aminotransferase levels

ASMER1 · rs7280197

What the study found

Who was studied 1,010,710 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0028 higher (95% confidence interval 0.002-0.0036); p = 2 × 10−12.

Where it sits Chromosome 21, band 21q21.1 — in an intron of ASMER1.

What each result means

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

Questions about rs7280197

What is rs7280197?

rs7280197 is a single position in the genome, in or near the ASMER1 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 rs7280197 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 rs7280197 come from?

GWAS Catalog, Nature genetics 2024, PMID:38632349. 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.

Alanine aminotransferase levels (rs7280197). MyGeneLog™. https://www.mygenelog.com/variants/rs7280197

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