rs387906789, VCP

N. diseases: 14
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 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
CUI: C3151403
Disease: AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
7 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.800 1.000 13 2005 2018
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1
CUI: C4551951
Disease: Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1
9 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.700 1.000 11 2005 2018
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.030 1.000 3 2009 2013
Osteitis Deformans
CUI: C0029401
Disease: Osteitis Deformans
58 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.030 0.667 3 2012 2018
Muscle Weakness
CUI: C0151786
Disease: Muscle Weakness
87 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.020 1.000 2 2009 2013
Myopathy
CUI: C0026848
Disease: Myopathy
166 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.020 0.500 2 2012 2018
Paresis
CUI: C0030552
Disease: Paresis
49 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.020 1.000 2 2009 2013
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2013 2013
Amyotrophic Lateral Sclerosis, Familial
CUI: C4551993
Disease: Amyotrophic Lateral Sclerosis, Familial
68 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2013 2013
Dementia
CUI: C0497327
Disease: Dementia
176 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2013 2013
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA
CUI: C1833662
Disease: INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA
6 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2012 2012
Inclusion Body Myopathy, Sporadic
CUI: C0751713
Disease: Inclusion Body Myopathy, Sporadic
5 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2016 2016
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2012 2012
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 0.010 1.000 1 2013 2013