发明名称 |
METHOD OF PROVIDING THE INFORMATION OF SINGLE NUCLEOTIDE POLYMORPHISM ASSOCIATED WITH RENAL FUNCTION RELATED TRAIT |
摘要 |
<p>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.</p> |
申请公布号 |
KR20130075420(A) |
申请公布日期 |
2013.07.05 |
申请号 |
KR20110143780 |
申请日期 |
2011.12.27 |
申请人 |
KOREA CENTER FOR DISEASE CONTROL AND PREVENTION |
发明人 |
GO, MIN JIN;KIM, YOUNG JIN;LEE, JONG YOUNG;CHO, YOON SHIN;HAN, BOK GHEE |
分类号 |
C12N15/11;C12Q1/68 |
主分类号 |
C12N15/11 |
代理机构 |
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代理人 |
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主权项 |
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地址 |
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