CPC C12Q 1/6883 (2013.01) [C12Q 2600/106 (2013.01); C12Q 2600/156 (2013.01); C12Q 2600/158 (2013.01)] | 8 Claims |
1. A method for detecting a T allele in a single nucleotide variation (SNV) in rs77150043 on 16q12.1 in ADCY7 in a Crohn's disease (CD) or psoriasis (PS or PSOR) human patient, the method comprising:
a) obtaining a biological sample from the human patient; and
b) detecting in a nucleic acid from the sample a T allele in SNV rs77150043 on 16q12.1 in ADCY7 by contacting the sample with a probe specific for said SNV and detecting binding between said probe and said SNV.
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