SLC22A3 · rs145846934
Where this position leads
Condition: Aortic Stenosis
What the study found
Who was studied 205,483 European ancestry individuals (MTAG effective sample size boosted by aortic valve function samples).
The effect Each copy of the A allele shifted the measure 0.0373 lower (95% confidence interval 0.027-0.048); p = 2 × 10−12.
How common The A allele had a frequency of about 85% in the people studied.
Where it sits Chromosome 6, band 6q25.3 — in an intron of SLC22A3.
rs145846934 is a single position in the genome, in or near the SLC22A3 gene. Published research associates it with aortic stenosis (mtag). 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 Aortic Stenosis. 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, Nature genetics 2026, PMID:41419685. 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.
Aortic stenosis (MTAG) (rs145846934). MyGeneLog™. https://www.mygenelog.com/variants/rs145846934