Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1424014997
rs1424014997
SOD1 ; SCAF4
0.020 GeneticVariation BEFREE In contrast, perturbations caused by the ALS mutation are completely masked in the crystal structure of I149T. 25296320

2014
dbSNP: rs1424014997
rs1424014997
SOD1 ; SCAF4
0.020 GeneticVariation BEFREE Clinical phenotypes of a large Chinese multigenerational kindred with autosomal dominant familial ALS due to Ile149Thr SOD1 gene mutation. 16963403

2006