Dan Roden
Faculty Member
Last active: 3/24/2020

A rare variant in MYH6 is associated with high risk of sick sinus syndrome.

Holm H, Gudbjartsson DF, Sulem P, Masson G, Helgadottir HT, Zanon C, Magnusson OT, Helgason A, Saemundsdottir J, Gylfason A, Stefansdottir H, Gretarsdottir S, Matthiasson SE, Thorgeirsson GM, Jonasdottir A, Sigurdsson A, Stefansson H, Werge T, Rafnar T, Kiemeney LA, Parvez B, Muhammad R, Roden DM, Darbar D, Thorleifsson G, Walters GB, Kong A, Thorsteinsdottir U, Arnar DO, Stefansson K
Nat Genet. 2011 43 (4): 316-20

PMID: 21378987 · PMCID: PMC3066272 · DOI:10.1038/ng.781

Through complementary application of SNP genotyping, whole-genome sequencing and imputation in 38,384 Icelanders, we have discovered a previously unidentified sick sinus syndrome susceptibility gene, MYH6, encoding the alpha heavy chain subunit of cardiac myosin. A missense variant in this gene, c.2161C>T, results in the conceptual amino acid substitution p.Arg721Trp, has an allelic frequency of 0.38% in Icelanders and associates with sick sinus syndrome with an odds ratio = 12.53 and P = 1.5 × 10⁻²⁹. We show that the lifetime risk of being diagnosed with sick sinus syndrome is around 6% for non-carriers of c.2161C>T but is approximately 50% for carriers of the c.2161C>T variant.

MeSH Terms (23)

Adult Aged Aged, 80 and over Cardiac Myosins Case-Control Studies Female Genetic Predisposition to Disease Genetic Variation Genome-Wide Association Study Heart Diseases Heart Rate Heterozygote Humans Iceland Male Middle Aged Mutation, Missense Myosin Heavy Chains Odds Ratio Oligonucleotide Array Sequence Analysis Penetrance Polymorphism, Single Nucleotide Sick Sinus Syndrome

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