SLC11A1, solute carrier family 11 member 1, 6556

N. diseases: 141; N. variants: 14
Disease: Crohn Disease ×
Source: ALL
Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs17235409
rs17235409
Entrez Id: 6556
Gene Symbol: SLC11A1
SLC11A1
CUI: C0010346
Disease:
Crohn Disease 		0.010 GeneticVariation BEFREE Three NRAMP1 polymorphisms [5'(GT)n, D543N, and INT4G/C] were significantly associated with CD. 18454481 2008