Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs1555836950
rs1555836950
SOD1 ; SCAF4
A 0.700 GeneticVariation CLINVAR A familial ALS case carrying a novel p.G147C SOD1 heterozygous missense mutation with non-executive cognitive impairment. 24769475

2014
dbSNP: rs1555836950
rs1555836950
SOD1 ; SCAF4
A 0.700 GeneticVariation CLINVAR Identify mutation in amyotrophic lateral sclerosis cases using HaloPlex target enrichment system. 25109764

2014
dbSNP: rs1555836950
rs1555836950
SOD1 ; SCAF4
A 0.700 GeneticVariation CLINVAR SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations. 20577002

2010