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Asparaginase hypersensitivity in acute lymphoblastic leukemia

HLA-DQA1 · rs28383308

Where this position leads

Condition: Acute Lymphoblastic Leukemia

rs28383308 Condition: Acute Lymphoblastic Leukemia Acute Lymphoblastic Leukemia Condition rs28383308 rs28383308 HLA-DQA1

What the study found

Who was studied 2,290 European ancestry individuals, 310 African ancestry individuals, 798 Native American individuals, 112 Asian ancestry individuals, 387 individuals.

The effect Each copy of the T allele carried 1.95 times the odds of Asparaginase hypersensitivity in acute lymphoblastic leukemia; p = 5 × 10−14.

Where it sits Chromosome 6, band 6p21.32 — between genes, 9.2 kb from HLA-DQA1.

What each result means

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

Questions about rs28383308

What is rs28383308?

rs28383308 is a single position in the genome, in or near the HLA-DQA1 gene. Published research associates it with asparaginase hypersensitivity in acute lymphoblastic leukemia. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

What conditions is rs28383308 linked to?

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

Does having rs28383308 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 rs28383308 come from?

GWAS Catalog, Clinical pharmacology and therapeutics 2021, PMID:33768542. 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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Asparaginase hypersensitivity in acute lymphoblastic leukemia (rs28383308). MyGeneLog™. https://www.mygenelog.com/variants/rs28383308

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