rs4722999, CRHR2

N. diseases: 5
Disease: Irritable Bowel Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Irritable Bowel Syndrome
CUI: C0022104
Disease: Irritable Bowel Syndrome
0.010 GeneticVariation BEFREE We found that rs4722999 and rs3779250, located in intronic region, were associated with IBS in terms of genotype frequency (rs4722999: P = 0.037; rs3779250: P = 0.017) and that the distribution of the major allele was significantly different between patients and controls. 26808377 2016