rs267606832, FUS

N. diseases: 3
Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder) ×
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
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