Sensitive

Thionamide-induced agranulocytosis in Graves' disease

HLA · rs9263688

Where this position leads

Condition: Graves' Disease

rs9263688 Condition: Graves' Disease Graves' Disease Condition rs9263688 rs9263688 HLA

What the study found

Who was studied 21 East Asian ancestry cases with agranulocytosis, 662 East Asian ancestry cases without agranulocytosis; replicated in 21 East Asian ancestry cases with agranulocytosis, 546 East Asian ancestry cases without agranulocytosis.

The effect The reported allele is G; the catalogue records no effect size ; p = 5 × 10−21.

How common The G allele had a frequency of about 5% in the people studied.

Where it sits Chromosome 6, band 6p21.33 — in an intron of PSORS1C1.

What each result means

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

Questions about rs9263688

What is rs9263688?

rs9263688 is a single position in the genome, in or near the HLA gene. Published research associates it with thionamide-induced agranulocytosis in graves' 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 rs9263688 linked to?

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

Does having rs9263688 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 rs9263688 come from?

GWAS Catalog, Nature communications 2015, PMID:26151496. 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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Thionamide-induced agranulocytosis in Graves' disease (rs9263688). MyGeneLog™. https://www.mygenelog.com/variants/rs9263688

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