SFXN1, sideroflexin 1, 94081

N. diseases: 73; N. variants: 1
Disease: Crohn Disease ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0010346
Disease: Crohn Disease
Crohn Disease 		0.010 GeneticVariation disease BEFREE The TCC allele at codon 35 of IL18 may increase the risk for Crohn's disease, especially in females. 12572878 2002