摘要 |
<p>The present invention provides a polynucleotide containing single-nucleotide polymorphism (SNP) for diagnosing susceptibility to Crohn′s disease, or a complementary polynucleotide. More specifically, provided is a polynucleotide marker composition for diagnosing susceptibility to crohn′s disease including: a polynucleotide composed of 10 to 50 continuous DNA sequence including twenty-seventh base (polymorphic region), as a polynucleotide where at least one species is selected from a cluster composed of 1 to 4 sequence number; or a complementary polynucleotide thereof. The polynucleotide or the complementary polynucleotide of the present invention can be usefully used in Crohn′s disease diagnosis, risk prediction of Crohn′s disease, etc. as a diagnostic marker of Crohn′s disease heredity.</p> |