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NAPRT protein levels

TIGD5 · rs111956838

Where this position leads

Condition: Celiac Disease

rs111956838 Condition: Celiac Disease Celiac Disease Condition rs111956838 rs111956838 TIGD5

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.156 higher (95% confidence interval 0.11-0.2); p = 8 × 10−12.

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

Where it sits Chromosome 8, band 8q24.3 — in the 3′ untranslated region of TIGD5.

What each result means

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

Questions about rs111956838

What is rs111956838?

rs111956838 is a single position in the genome, in or near the TIGD5 gene. Published research associates it with naprt 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 rs111956838 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 rs111956838 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 rs111956838 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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NAPRT protein levels (rs111956838). MyGeneLog™. https://www.mygenelog.com/variants/rs111956838

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