Methods for Detecting an increased risk for coronary heart disease
AssigneeBoard of Regents, The University of Texas System
InventorsJonathan C. Cohen, Helen H. Hobbs
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AssigneeBoard of Regents, The University of Texas System
InventorsJonathan C. Cohen, Helen H. Hobbs
Estimating the term…
The invention relates generally to an allele on human chromosome 9 associated with increased risk for coronary heart disease and the use or detection of such an allele in determining whether a human has an increased risk for coronary heart disease. In one aspect, the invention relates to methods for detecting a predisposition or propensity or susceptibility for coronary heart disease in a human, comprising detecting the presence of an allele on human chromosome 9 that is associated with an increased risk for coronary heart disease in a human. Disclosed are methods and compositions for determining whether a person carries an allele associated with increased risk for coronary atherosclerosis by determining whether the person has an RA-CHR9 allele, such as by determining whether the person has an RA-CHR9 allele-associated single nucleotide polymorphism (SNP). The invention also relates to kits for detecting the presence of an allele on chromosome 9 associated with an increased risk for coronary heart disease.
A method for determining treatment of a person for increased risk for coronary heart disease, the method comprising steps:
A method for tailoring healthcare treatment of a person, the method comprising steps:
Dependencies are inferred from the claim text.