rs267606832, FUS

N. diseases: 3
Source: ALL
Disease Risk Allele Score vda Association Type Original DB Sentence supporting the association PMID PMID Year
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
CUI: C1842675
Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Screening of SOD1, FUS and TARDBP genes in patients with amyotrophic lateral sclerosis in central-southern China. 27604643 2016
TREMOR, HEREDITARY ESSENTIAL, 4
CUI: C3539195
Disease: TREMOR, HEREDITARY ESSENTIAL, 4
0.800 GeneticVariation UNIPROT Exome sequencing identifies FUS mutations as a cause of essential tremor. 22863194 2012
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
CUI: C1842675
Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations of FUS gene in sporadic amyotrophic lateral sclerosis. 19861302 2010
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
CUI: C1842675
Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Genetic contribution of FUS to frontotemporal lobar degeneration. 20124201 2010
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
CUI: C1842675
Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations in the FUS/TLS gene on chromosome 16 cause familial amyotrophic lateral sclerosis. 19251627 2009
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
CUI: C1842675
Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 GeneticVariation UNIPROT Mutations in FUS, an RNA processing protein, cause familial amyotrophic lateral sclerosis type 6. 19251628 2009
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
CUI: C1842675
Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
0.800 CausalMutation CLINVAR
TREMOR, HEREDITARY ESSENTIAL, 4
CUI: C3539195
Disease: TREMOR, HEREDITARY ESSENTIAL, 4
0.800 CausalMutation CLINVAR
Essential Tremor
CUI: C0270736
Disease: Essential Tremor
0.010 GeneticVariation BEFREE In addition, two other rare FUS variants were identified (p.R216C and p.P431L) in Essential Tremor patients however co-segregation analysis with disease was not possible. 23601511 2013