| 摘要 |
<p>In the present invention, provided is a polynucleotide including a single-nucleotide polymorphis (SNP) for diagnosing the susceptibility to Crohn′s disease or a complementary polynucleotide thereof. More specifically, provided is a marker composition for diagnosing the susceptibility to Crohn′s disease including at least one type of polynucleotide selected from the group consisting of sequence numbers 1 to 4, wherein the polynucleotide has 10-50 serial DNA sequences including the 27^th base (polymorphism area) or complementary polynucleotide thereof. The polynucleotide or complementary polynucleotide thereof, according to the present invention, can be used for diagnosing Crohn′s disease and predicting Crohn′s disease risk as a hereditary diagnosis sign.</p> |
