rs121909668, FUS

N. diseases: 8
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
CUI: C1842675
Disease: AMYOTROPHIC LATERAL SCLEROSIS 6 (disorder)
67 0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 0.800 1.000 13 2009 2016
TREMOR, HEREDITARY ESSENTIAL, 4
CUI: C3539195
Disease: TREMOR, HEREDITARY ESSENTIAL, 4
4 0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 0.700 1.000 9 2009 2014
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 0.090 1.000 9 2010 2017
AMYOTROPHIC LATERAL SCLEROSIS 1
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
139 0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 0.030 1.000 3 2010 2014
Amyotrophic Lateral Sclerosis, Familial
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
68 0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 0.010 1.000 1 2012 2012
Cognition Disorders
CUI: C0009241
Disease: Cognition Disorders
47 0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 0.010 1.000 1 2018 2018
Dropped head syndrome
CUI: C3266164
Disease: Dropped head syndrome
1 0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 0.010 1.000 1 2010 2010
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.790 0.120 16 31191418 missense variant C/A;G;T snv 1.2E-05 0.010 1.000 1 2018 2018