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Independent Susceptibility Markers for Atrial Fibrillation on Chromosome 4q25
Author(s) -
Steven A. Lubitz,
Moritz F. Sinner,
Kathryn L. Lunetta,
Seiko Makino,
Arne Pfeufer,
Rosanna Rahman,
Caroline E. Veltman,
John Barnard,
Joshua C. Bis,
Stephan P. Danik,
Akshata Sonni,
Marisa A. Shea,
Federica del Monte,
Siegfried Perz,
Martina MüllerNurasyid,
Annette Peters,
Steven M. Greenberg,
Karen L. Furie,
Charlotte van Noord,
Eric Boerwinkle,
Bruno H. Stricker,
Jacqueline C.M. Witteman,
Jonathan D. Smith,
Mina K. Chung,
Susan R. Heckbert,
Emelia J. Benjamin,
Jonathan Rosand,
Dan E. Arking,
Álvaro Alonso,
Stefan Kääb,
Patrick T. Ellinor
Publication year - 2010
Publication title -
circulation
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 7.795
H-Index - 607
eISSN - 1524-4539
pISSN - 0009-7322
DOI - 10.1161/circulationaha.109.886440
Subject(s) - single nucleotide polymorphism , odds ratio , locus (genetics) , genetics , snp , medicine , minor allele frequency , rotterdam study , haplotype , allele , confidence interval , case control study , genetic predisposition , genotype , bioinformatics , biology , gene
Genetic variants on chromosome 4q25 are associated with atrial fibrillation (AF). We sought to determine whether there is more than 1 susceptibility signal at this locus.

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