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Stands on its own.
Nothing else here links to this position yet — but the page above is the point: what the
research found, what each genotype means, and where it came from, in language you can
read. Links to conditions, drugs and the senses appear automatically if we write them.
What the study found
Who was studied 118,780 European ancestry, African ancestry, Hispanic or Latin American individuals.
The effect
Each copy of the A allele shifted the measure 0.034 lower (95% confidence interval 0.026-0.042); p = 2 × 10−15.
How common The A allele had a frequency of about 42% in the people studied.
Where it sits Chromosome 2, band 2p23.3 — in an intron of DPYSL5.
What each result means
A/ATwo copies of the version the research linked to Spatial QRS-T angle. That is the strongest link of the three results. A link in a study is not a diagnosis.
A/GOne copy of the version the research linked to Spatial QRS-T angle. That is a smaller link than two copies.
G/GNo copy of the version the research linked to Spatial QRS-T angle. This is the starting point the study compared everyone against.
Nature communications · 2023 · PMID 36918541 · open access
Questions about rs13029206
What is rs13029206?
rs13029206 is a single position in the genome, in or near the DPYSL5 gene. Published research associates it with spatial qrs-t angle. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.
Does having rs13029206 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 rs13029206 come from?
GWAS Catalog, Nature communications 2023, PMID:36918541. 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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