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CA5A protein levels

SLC7A5-AS1 · rs188359514

Where this position leads

Condition: Celiac Disease

rs188359514 Condition: Celiac Disease Celiac Disease Condition rs188359514 rs188359514 SLC7A5-AS1

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.13 lower (95% confidence interval 0.09-0.169); p = 5 × 10−12.

How common The T allele had a frequency of about 2% in the people studied.

Where it sits Chromosome 16, band 16q24.2 — in an intron of SLC7A5-AS1.

What each result means

C/C No copy of the version the research linked to CA5A protein levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to CA5A protein levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to CA5A protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs188359514

What is rs188359514?

rs188359514 is a single position in the genome, in or near the SLC7A5-AS1 gene. Published research associates it with ca5a 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 rs188359514 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 rs188359514 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 rs188359514 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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CA5A protein levels (rs188359514). MyGeneLog™. https://www.mygenelog.com/variants/rs188359514

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