rs11563648 - PRELID3BP10 - ZNF800
Magnitude 2.2 · 1 study on file
Reported associations
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Identification of genomic loci associated with resting heart rate and shared genetic predictors with all-cause mortality. - Nature genetics (2017) · Eppinga RN, Hagemeijer Y, Burgess S, Hinds DA, Stefansson K, Gudbjartsson DF, van Veldhuisen DJ, Munroe PB, Verweij N, van der Harst P · PubMed 27798624
Resting heart rate is a heritable trait correlated with life span. Little is known about the genetic contribution to resting heart rate and its relationship with mortality. We performed a genome-wide association discovery and replication analysis starting with 19.9 million genetic variants and studying up to 265,046 individuals to identify 64 loci associated with resting heart rate (P < 5 × 10 ); 46 of these were novel. We then used the genetic variants identified to study the association between resting heart rate and all-cause mortality. We observed that a genetically predicted resting heart rate increase of 5 beats per minute was associated with a 20% increase in mortality risk (hazard ratio 1.20, 95% confidence interval 1.11-1.28, P = 8.20 × 10 ) translating to a reduction in life ex
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Lifestyle context
Concrete actions anchored to the cited research. We do not prescribe, we describe.
Screening
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Resting heart rate measurement Moderate
rs11563648-C allele is associated with elevated resting heart rate; baseline and periodic measurement establishes status relative to this genetic contribution.
Obtain resting heart rate at baseline and annually during health checkups.