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Who was studied 15,124 Hispanic or Latin American individuals.
The effect
Each copy of the A allele shifted the measure 0.77 ms higher (95% confidence interval 0.52-1.02); p = 8 × 10−10.
How common The A allele had a frequency of about 19% in the people studied.
Where it sits Chromosome 10, band 10q25.2 — in an intron of VTI1A.
What each result means
A/ATwo copies of the version the research linked to QRS duration. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/COne copy of the version the research linked to QRS duration. That is a smaller link than two copies.
C/CNo copy of the version the research linked to QRS duration. This is the starting point the study compared everyone against.
rs7906312 is a single position in the genome, in or near the VTI1A 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.
What conditions is rs7906312 linked to?
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.
Does having rs7906312 mean I will get this?
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.
Where does the information about rs7906312 come from?
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.
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