HLA-B · rs2257269
Where this position leads
Drugs: Abacavir, Allopurinol, Carbamazepine and oxcarbazepine, Lamotrigine (Lamictal)
Strength of the evidence
Its strongest genetic-study result is p = 10−8, with 1 associations in the GWAS Catalog.
4: ClinVar disease-causing, reviewed by an expert panel or a guideline (3–4 stars). 3: ClinVar, several labs agreeing (2 stars), or a genetic study at p ≤ 10−50. 2: ClinVar from one lab (1 star), or p ≤ 10−20. 1: ClinVar submitted without criteria (0 stars), or genome-wide significance (p ≤ 5×10−8). The higher of the two counts. It says how solid the evidence is, not whether it matters for a particular person.
What the study found
Who was studied 219,872 British ancestry women.
The effect Each copy of the A allele shifted the measure 0.0159 higher (95% confidence interval 0.01-0.022); p = 3 × 10−8.
Where it sits Chromosome 6, band 6p21.33 — a synonymous change in HLA-B.
rs2257269 is a single position in the genome, in or near the HLA-B gene. Published research associates it with a body shape index. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
HLA-B carries pharmacogenomic findings for Abacavir, Allopurinol, Carbamazepine and oxcarbazepine, Lamotrigine (Lamictal). That is educational information, not a prescription or a dosing guide. Any decision to start, stop or change a medicine belongs with the clinician or pharmacist managing your treatment.
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.
GWAS Catalog, Scientific reports 2021, PMID:34021172. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
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A body shape index (rs2257269). MyGeneLog™. https://www.mygenelog.com/variants/rs2257269