rs4880, SOD2

N. diseases: 131
Disease: Adrenoleukodystrophy ×
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
Adrenoleukodystrophy
CUI: C0162309
Disease: Adrenoleukodystrophy
0.010 GeneticVariation BEFREE There was no association between childhood cerebral XALD and the C47T variant or the GTAC haplotype. 22218650 2012