Source: ALL
Variant Gene Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
dbSNP: rs121909668
rs121909668
FUS
G 0.700 CausalMutation CLINVAR Extensive molecular genetic survey of Taiwanese patients with amyotrophic lateral sclerosis. 24908169

2014
dbSNP: rs121909668
rs121909668
FUS
G 0.700 CausalMutation CLINVAR Activity-dependent FUS dysregulation disrupts synaptic homeostasis. 25324524

2014
dbSNP: rs121909668
rs121909668
FUS
G 0.700 CausalMutation CLINVAR Characterization of FUS mutations in amyotrophic lateral sclerosis using RNA-Seq. 23577159

2013
dbSNP: rs121909668
rs121909668
FUS
G 0.700 CausalMutation CLINVAR ALS-associated FUS mutations result in compromised FUS alternative splicing and autoregulation. 24204307

2013
dbSNP: rs121909668
rs121909668
FUS
G 0.700 CausalMutation CLINVAR FUS mutations in sporadic amyotrophic lateral sclerosis: clinical and genetic analysis. 22055719

2012
dbSNP: rs121909668
rs121909668
FUS
G 0.700 CausalMutation CLINVAR SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype-phenotype correlations. 20577002

2010
dbSNP: rs121909668
rs121909668
FUS
G 0.700 CausalMutation CLINVAR Frameshift and novel mutations in FUS in familial amyotrophic lateral sclerosis and ALS/dementia. 20668259

2010
dbSNP: rs121909668
rs121909668
FUS
G 0.700 CausalMutation CLINVAR ALS-associated fused in sarcoma (FUS) mutations disrupt Transportin-mediated nuclear import. 20606625

2010
dbSNP: rs121909668
rs121909668
FUS
G 0.700 CausalMutation CLINVAR Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. 19251627

2009