Standard

QT interval

ATP1B1 · rs1983546

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

A/A Published research associates this genotype with typical/baseline likelihood of QT interval — no copies of the reported risk allele. (GWAS Catalog, Nat Genet 2014, PMID:24952745)
A/G Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with QT interval. (GWAS Catalog, Nat Genet 2014, PMID:24952745)
G/G Published research associates this genotype (two copies of the reported risk allele) with a higher likelihood of QT interval compared to the general population. (GWAS Catalog, Nat Genet 2014, PMID:24952745)

Source: GWAS Catalog, Nat Genet 2014, PMID:24952745

Questions about rs1983546

What is rs1983546?

rs1983546 is a single position in the genome, in or near the ATP1B1 gene. Published research associates it with qt interval. A single variant does not decide an outcome — it shifts a probability, and for most common variants the shift is small.

Does having rs1983546 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 rs1983546 come from?

GWAS Catalog, Nat Genet 2014, PMID:24952745. 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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