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GAL protein levels

MARK4 · rs77660932

Where this position leads

Condition: Celiac Disease

rs77660932 Condition: Celiac Disease Celiac Disease Condition rs77660932 rs77660932 MARK4

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the C allele shifted the measure 0.0404 lower (95% confidence interval 0.027-0.054); p = 6 × 10−12.

How common The C allele had a frequency of about 16% in the people studied.

Where it sits Chromosome 19, band 19q13.32 — in a regulatory region of MARK4.

What each result means

C/C Two copies of the version the research linked to GAL protein 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 GAL protein levels. That is a smaller link than two copies.
T/T No copy of the version the research linked to GAL protein levels. This is the starting point the study compared everyone against.
Source

Questions about rs77660932

What is rs77660932?

rs77660932 is a single position in the genome, in or near the MARK4 gene. Published research associates it with gal protein levels. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs77660932 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 rs77660932 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 rs77660932 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

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GAL protein levels (rs77660932). MyGeneLog™. https://www.mygenelog.com/variants/rs77660932

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