rs17235409, SLC11A1

N. diseases: 31
Disease: Behcet Syndrome ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
0.020 GeneticVariation BEFREE We analyzed the association of NRAMP1 polymorphisms [(GT)( n ), INT4, 3'UTR and D543N] in 102 Turkish patients with BS and 102 healthy subjects by using amplification refractory mutation system-polymerase chain reaction (ARMS-PCR). 18998137 2009
Behcet Syndrome
CUI: C0004943
Disease: Behcet Syndrome
0.020 GeneticVariation BEFREE In addition, the distributions of genotypes and alleles of D543N were similar between BD patients and controls (p>0.05). 17062442 2006