Source: ALL

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2234694
rs2234694
SOD1
0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02
CUI: C0011881
Disease: Diabetic Nephropathy
Diabetic Nephropathy 		0.010 1.000 1 2010 2010
dbSNP: rs2234694
rs2234694
SOD1
0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02
CUI: C0024117
Disease: Chronic Obstructive Airway Disease
Chronic Obstructive Airway Disease 		0.010 1.000 1 2019 2019
dbSNP: rs2234694
rs2234694
SOD1
0.882 0.240 21 31666552 intron variant A/C snv 3.6E-02 3.4E-02
CUI: C0011854
Disease: Diabetes Mellitus, Insulin-Dependent
Diabetes Mellitus, Insulin-Dependent 		0.010 1.000 1 2010 2010
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.100 1.000 30 1995 2020
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1 		0.800 1.000 20 1993 2009
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C0085084
Disease: Motor Neuron Disease
Motor Neuron Disease 		0.030 1.000 3 1996 2006
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
Amyotrophic Lateral Sclerosis, Familial 		0.030 1.000 3 1998 2001
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C1862941
Disease: Amyotrophic Lateral Sclerosis, Sporadic
Amyotrophic Lateral Sclerosis, Sporadic 		0.020 1.000 2 1996 2010
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C1839259
Disease: Bulbo-Spinal Atrophy, X-Linked
Bulbo-Spinal Atrophy, X-Linked 		0.010 1.000 1 2010 2010
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2005 2005
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C0030552
Disease: Paresis
Paresis 		0.010 1.000 1 2001 2001
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C4509818
Disease: Facial onset sensory and motor neuronopathy syndrome
Facial onset sensory and motor neuronopathy syndrome 		0.010 1.000 1 2014 2014
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C3539781
Disease: Progressive cGVHD
Progressive cGVHD 		0.010 1.000 1 2005 2005
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C0677932
Disease: Progressive Neoplastic Disease
Progressive Neoplastic Disease 		0.010 1.000 1 2005 2005
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C0026769
Disease: Multiple Sclerosis
Multiple Sclerosis 		0.010 1.000 1 2001 2001
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C1611743
Disease: Familial (FPAH)
Familial (FPAH) 		0.010 1.000 1 1996 1996
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C0221505
Disease: Lesion of brain
Lesion of brain 		0.010 1.000 1 2005 2005
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C0234985
Disease: Mental deterioration
Mental deterioration 		0.010 1.000 1 2005 2005
dbSNP: rs80265967
rs80265967
SOD1
0.732 0.200 21 31667290 missense variant A/C;T snv 1.4E-03 1.2E-03
CUI: C3542025
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE
AMYOTROPHIC LATERAL SCLEROSIS 1, AUTOSOMAL RECESSIVE 		0.700 0
dbSNP: rs121912443
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1 		0.890 1.000 40 1993 2014
dbSNP: rs121912435
rs121912435
SOD1
0.925 0.080 21 31663848 missense variant A/G snv 4.0E-06
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1 		0.810 1.000 27 1993 2012
dbSNP: rs121912439
rs121912439
SOD1
0.851 0.080 21 31667320 missense variant A/G snv
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
AMYOTROPHIC LATERAL SCLEROSIS 1 		0.810 1.000 24 1993 2012
dbSNP: rs121912443
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
Amyotrophic Lateral Sclerosis 		0.100 0.917 12 1994 2017
dbSNP: rs121912443
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
Amyotrophic Lateral Sclerosis, Familial 		0.100 1.000 12 1994 2005
dbSNP: rs121912443
rs121912443
SOD1
0.732 0.160 21 31663857 missense variant A/G snv
CUI: C0700095
Disease: Central neuroblastoma
Central neuroblastoma 		0.030 1.000 3 1999 2007