Standard

PR segment duration

ARHGAP24 · rs13137008

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 each result means

G/G Published research associates this genotype with typical/baseline likelihood of PR segment duration — no copies of the reported risk allele.

G/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with PR segment duration.

T/T Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of PR segment duration compared to the general population.

Source

Genetic determinants of P wave duration and PR segment

Verweij N, Mateo Leach I, van den Boogaard M, van Veldhuisen DJ, Christoffels VM, Hillege HL, van Gilst WH, Barnett P, de Boer RA, van der Harst P

LifeLines Cohort Study

Circulation. Cardiovascular genetics · 2014 · PMID 24850809

Questions about rs13137008

What is rs13137008?

rs13137008 is a single position in the genome, in or near the ARHGAP24 gene. Published research associates it with pr segment duration. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs13137008 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 rs13137008 come from?

GWAS Catalog, Circ Cardiovasc Genet 2014, PMID:24850809. 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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