Standard

QT interval

NOS1AP · rs73017364

Where this position leads

Condition: QT Interval and Drug-Induced Long QT

Drug: QT-prolonging medicines

rs73017364 Condition: QT Interval and Drug-Induced Long QT QT Interval and Drug-Induced Long QT Condition Drug: QT-prolonging medicines QT-prolonging medicines Drug rs73017364 rs73017364 NOS1AP

What each result means

C/C Published research associates this genotype with typical/baseline likelihood of QT interval — no copies of the reported risk allele. (GWAS Catalog, Sci Rep 2017, PMID:29213071)
C/T Published research associates this genotype (one copy of the reported risk allele) with an intermediate association with QT interval. (GWAS Catalog, Sci Rep 2017, PMID:29213071)
T/T 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, Sci Rep 2017, PMID:29213071)

Source: GWAS Catalog, Sci Rep 2017, PMID:29213071

Questions about rs73017364

What is rs73017364?

rs73017364 is a single position in the genome, in or near the NOS1AP 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.

What conditions is rs73017364 linked to?

On MyGeneLog this position is linked to QT Interval and Drug-Induced Long QT. The research behind each link, and its sources, are set out on that condition page.

Does rs73017364 affect how medicines work?

NOS1AP carries pharmacogenomic findings for QT-prolonging medicines. That is educational information, not a prescription or a dosing guide. Any decision to start, stop or change a medicine belongs with the clinician or pharmacist managing your treatment.

Does having rs73017364 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 rs73017364 come from?

GWAS Catalog, Sci Rep 2017, PMID:29213071. 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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