Source: ALL

Variant Gene Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs4880
rs4880
SOD2
CUI: C0162309
Disease: Adrenoleukodystrophy
Adrenoleukodystrophy 		0.010 GeneticVariation BEFREE There was no association between childhood cerebral XALD and the C47T variant or the GTAC haplotype. 22218650

2012