Standard

Aspartate aminotransferase levels (UKB data field 30650)

near CACNB2 · rs139355580

Where this position leads

Condition: Celiac Disease

rs139355580 Condition: Celiac Disease Celiac Disease Condition rs139355580 rs139355580 near CACNB2

What the study found

Who was studied 394,642 European ancestry individuals.

The effect Each copy of the G allele shifted the measure 0.0806 higher (95% confidence interval 0.057-0.104); p = 7 × 10−12.

How common The G allele had a frequency of about 1% in the people studied.

Where it sits Chromosome 10, band 10p12.33 — between genes, 21 kb from CACNB2.

What each result means

A/A No copy of the version the research linked to Aspartate aminotransferase levels (UKB data field 30650). This is the starting point the study compared everyone against.
A/G One copy of the version the research linked to Aspartate aminotransferase levels (UKB data field 30650). That is a smaller link than two copies.
G/G Two copies of the version the research linked to Aspartate aminotransferase levels (UKB data field 30650). That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs139355580

What is rs139355580?

rs139355580 is a single position in the genome, in or near the near CACNB2 gene. Published research associates it with aspartate aminotransferase levels (ukb data field 30650). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs139355580 linked to?

On MyGeneLog this position is linked to Celiac Disease. The research behind each link, and its sources, are set out on that condition page.

Does having rs139355580 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 rs139355580 come from?

GWAS Catalog, Nature genetics 2025, PMID:39789286. 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.

Aspartate aminotransferase levels (UKB data field 30650) (rs139355580). MyGeneLog™. https://www.mygenelog.com/variants/rs139355580

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