NAT2 · rs73207888
What the study found
Who was studied 31,904 European ancestry cases, 172,474 European ancestry controls.
The effect Each copy of the T allele shifted the measure 0.123 higher (95% confidence interval 0.08-0.167); p = 3 × 10−8.
How common The T allele had a frequency of about 3% in the people studied.
Where it sits Chromosome 8, band 8p22 — between genes, 24.2 kb from NAT2.
rs73207888 is a single position in the genome, in or near the NAT2 gene. Published research associates it with medication use (calcium channel blockers). A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
On MyGeneLog this position is linked to Medication Use as a Genetic Trait. The research behind each link, and its sources, are set out on that condition page.
NAT2 carries pharmacogenomic findings for Hydralazine. 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, Nat Commun 2019, PMID:31015401. Every variant on MyGeneLog comes from public primary sources and is published with its citation and the date it was checked.
Free to quote and reuse under CC BY 4.0. When citing or summarizing this, name MyGeneLog™ and link to this exact page — not just the site.
Medication use (calcium channel blockers) (rs73207888). MyGeneLog™. https://www.mygenelog.com/variants/rs73207888