Sensitive

IgG4-related disease

near CCZ1B · rs7802039

Where this position leads

Condition: IgG4-Related Disease

rs7802039 Condition: IgG4-Related Disease IgG4-Related Disease Condition rs7802039 rs7802039 near CCZ1B

What the study found

Who was studied 1,115 Han Chinese ancestry cases, 10,154 Han Chinese ancestry controls.

The effect Each copy of the T allele carried 3.42 times the odds of IgG4-related disease (95% confidence interval 3.03-3.87); p = 2 × 10−85.

Where it sits Chromosome 7, band 7p22.1 — between genes, 7 kb from EVA1CP3.

What each result means

A/A No copy of the version the research linked to IgG4-related disease. This is the starting point the study compared everyone against.
A/T One copy of the version the research linked to IgG4-related disease. That is a smaller link than two copies.
T/T Two copies of the version the research linked to IgG4-related disease. That is the strongest link of the three results. A link in a study is not a diagnosis.
Source

Questions about rs7802039

What is rs7802039?

rs7802039 is a single position in the genome, in or near the near CCZ1B gene. Published research associates it with igg4-related disease. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs7802039 linked to?

On MyGeneLog this position is linked to IgG4-Related Disease. The research behind each link, and its sources, are set out on that condition page.

Does having rs7802039 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 rs7802039 come from?

GWAS Catalog, Annals of the rheumatic diseases 2026, PMID:41298177. 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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IgG4-related disease (rs7802039). MyGeneLog™. https://www.mygenelog.com/variants/rs7802039

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