SLC11A1, solute carrier family 11 member 1, 6556

N. diseases: 141; N. variants: 14
Disease: Behcet Syndrome ×
Source: ALL
Disease Score gda Association Type Type Original DB Sentence supporting the association PMID PMID Year
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.020 Biomarker disease BEFREE Our study suggests that NRAMP1 may be one of the plausible candidate genes for BS. 18998137 2009
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.020 GeneticVariation disease LHGDN SLC11A1 gene polymorphisms in Korean patients with Behçet's disease. 17062442 2006
CUI: C0004943
Disease: Behcet Syndrome
Behcet Syndrome 		0.020 GeneticVariation disease BEFREE The allele 3 and the genotype allele 3/allele 3 of the 5'-promoter (GT)n in the SLC11A1 gene may have a protective effect for the development of BD in the Korean population. 17062442 2006