SCN5A · rs62241190
Where this position leads
Condition: Cardiac Conduction Intervals (PR Interval and QRS Duration)
What the study found
Who was studied 15,124 Hispanic or Latin American individuals.
The effect Each copy of the G allele shifted the measure 2.46 ms higher (95% confidence interval 1.93-2.99); p = 6 × 10−20.
How common The G allele had a frequency of about 4% in the people studied.
Where it sits Chromosome 3, band 3p22.2 — in an intron of SCN5A.
rs62241190 is a single position in the genome, in or near the SCN5A gene. Published research associates it with qrs duration. 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 Cardiac Conduction Intervals (PR Interval and QRS Duration). 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, PloS one 2019, PMID:31251759. 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.
QRS duration (rs62241190). MyGeneLog™. https://www.mygenelog.com/variants/rs62241190