Disease: Myasthenia Gravis ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17209237
rs17209237
Entrez Id: 2908
Gene Symbol: NR3C1
NR3C1
CUI: C0026896
Disease:
Myasthenia Gravis 		0.010 GeneticVariation BEFREE rs17209237 in the GR gene was identified as an independent factor that contributes to GC efficacy in MG patients. 27185333 2016