RXFP2 · rs7983337
Where this position leads
Condition: Medication Use as a Genetic Trait
What the study found
Who was studied 31,904 European ancestry cases, 172,474 European ancestry controls.
The effect Each copy of the C allele shifted the measure 0.0773 lower (95% confidence interval 0.061-0.093); p = 1 × 10−21.
How common The C allele had a frequency of about 49% in the people studied.
Where it sits Chromosome 13, band 13q13.1 — between genes, 132.1 kb from RXFP2.
rs7983337 is a single position in the genome, in or near the RXFP2 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.
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) (rs7983337). MyGeneLog™. https://www.mygenelog.com/variants/rs7983337