rs74315452, SOD1

N. diseases: 12
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 1
CUI: C1862939
Disease: AMYOTROPHIC LATERAL SCLEROSIS 1
139 0.732 0.160 21 31667356 missense variant T/C snv 0.810 1.000 24 1993 2012
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.732 0.160 21 31667356 missense variant T/C snv 0.070 1.000 7 1997 2015
Amyotrophic Lateral Sclerosis, Familial
68 0.732 0.160 21 31667356 missense variant T/C snv 0.040 1.000 4 1999 2015
Adult Glioblastoma
CUI: C0278878
Disease: Adult Glioblastoma
98 0.732 0.160 21 31667356 missense variant T/C snv 0.010 1.000 1 2004 2004
Alzheimer's Disease
CUI: C0002395
Disease: Alzheimer's Disease
1843 0.732 0.160 21 31667356 missense variant T/C snv 0.010 1.000 1 2015 2015
Amyotrophic Lateral Sclerosis, Sporadic
90 0.732 0.160 21 31667356 missense variant T/C snv 0.010 1.000 1 2014 2014
Childhood Glioblastoma
CUI: C0280474
Disease: Childhood Glioblastoma
98 0.732 0.160 21 31667356 missense variant T/C snv 0.010 1.000 1 2004 2004
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.732 0.160 21 31667356 missense variant T/C snv 0.010 1.000 1 1997 1997
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.732 0.160 21 31667356 missense variant T/C snv 0.010 1.000 1 2012 2012
Glioblastoma
CUI: C0017636
Disease: Glioblastoma
281 0.732 0.160 21 31667356 missense variant T/C snv 0.010 1.000 1 2004 2004
Glioblastoma Multiforme
CUI: C1621958
Disease: Glioblastoma Multiforme
186 0.732 0.160 21 31667356 missense variant T/C snv 0.010 1.000 1 2004 2004
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.732 0.160 21 31667356 missense variant T/C snv 0.010 1.000 1 2012 2012