rs6189, NR3C1

N. diseases: 6
Disease: Eating Disorders ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Eating Disorders
CUI: C0013473
Disease: Eating Disorders
0.010 GeneticVariation BEFREE We studied whether genetic variants, such as N363S (rs56149945), exon 9-β (rs6198), ER22/23EK (rs6189-6190), and the intronic BclI restriction site (rs41423247) polymorphisms in the GR gene, could be considered as risk factors for the development of EDs and obesity in Italian patients. 20440229 2010