PURPOSE: A method for providing information of single nucleotide polymorphism (SNP) related to a renal function is provided to diagnose or predict diseases related to albumin and blood urea nitrogen (BUN) and to realize personalized medicine and predictive medicine through disease-related genetic information using the SNP marker. CONSTITUTION: A kit for diagnosing or predicting hearth diseases, atherosclerosis, or renal diseases contains a primer set which is complementary to SNP rs2280401 or rs6569474. The prediction or diagnosis is applied to Korean, Japanese, or Chinese. A method for diagnosing or predicting heart diseases, atherosclerosis, or renal diseases related to quantitative change of blood urea nitrogen comprises the step of identifying SNP rs2280401 or rs6569474 in DNA from an individual.
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