Methods and compositions for correlating genetic markers with cardiovascular disease

Abstract

The present invention provides methods of identifying a subject having an increased or decreased risk of developing cardiovascular disease, comprising: a) correlating the presence of one or more genetic markers in chromosome 3q13.31 with an increased or decreased risk of developing cardiovascular disease; and b) detecting the one or more genetic markers of step (a) in the subject, thereby identifying the subject as having an increased or decreased risk of developing cardiovascular disease. Also provided are methods of identifying subjects with cardiovascular disease as having a good or poor prognosis, as well as methods of identifying effective treatment regimens for cardiovascular disease, based on correlation with genetic markers in chromosome 3q13.31.

1 - 2 . (canceled) 
     
     
         3 . A method of identifying a human subject having an increased risk of developing coronary artery disease, comprising detecting in a nucleic acid sample obtained from the subject an A allele at single nucleotide polymorphism rs1910040, wherein detection of said allele identifies the subject as having an increased risk of developing coronary artery disease. 
     
     
         4 . The method of  claim 3 , wherein detecting is carried out by a hybridization reaction. 
     
     
         5 . The method of  claim 4 , wherein the hybridization reaction is carried out with hybridization probes in a microarray. 
     
     
         6 . The method of  claim 3 , wherein detecting is carried out by electrophoresis. 
     
     
         7 . The method of  claim 3 , wherein detecting is carried out by restriction endonuclease digestion analysis. 
     
     
         8 . The method of  claim 3 , wherein detecting is carried out by an amplification reaction. 
     
     
         9 . The method of  claim 8 , wherein the amplification reaction is a polymerase chain reaction.