Disease: Irritable Bowel Syndrome ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs3779250
rs3779250
Entrez Id: 1395
Gene Symbol: CRHR2
CRHR2
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
dbSNP: rs4722999
rs4722999
Entrez Id: 1395
Gene Symbol: CRHR2
CRHR2
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