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HSBP1 protein levels

PSMB9 · rs3763348

Where this position leads

Condition: Celiac Disease

rs3763348 Condition: Celiac Disease Celiac Disease Condition rs3763348 rs3763348 PSMB9

What the study found

Who was studied 47,745 European ancestry individuals.

The effect Each copy of the T allele shifted the measure 0.0362 lower (95% confidence interval 0.025-0.047); p = 4 × 10−13.

How common The T allele had a frequency of about 42% in the people studied.

Where it sits Chromosome 6, band 6p21.32 — in an intron of PSMB9.

What each result means

C/C No copy of the version the research linked to HSBP1 protein levels. This is the starting point the study compared everyone against.
C/T One copy of the version the research linked to HSBP1 protein levels. That is a smaller link than two copies.
T/T Two copies of the version the research linked to HSBP1 protein levels. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs3763348

What is rs3763348?

rs3763348 is a single position in the genome, in or near the PSMB9 gene. Published research associates it with hsbp1 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 rs3763348 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 rs3763348 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 rs3763348 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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HSBP1 protein levels (rs3763348). MyGeneLog™. https://www.mygenelog.com/variants/rs3763348

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