rs121909335, VCP

N. diseases: 9
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.
Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1
9 0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 0.800 1.000 23 2004 2018
AMYOTROPHIC LATERAL SCLEROSIS 14 WITH OR WITHOUT FRONTOTEMPORAL DEMENTIA
7 0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 0.700 1.000 9 2005 2016
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 0.020 1.000 2 2012 2015
Osteitis Deformans
CUI: C0029401
Disease: Osteitis Deformans
58 0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 0.020 1.000 2 2009 2020
Amyotrophic Lateral Sclerosis
CUI: C0002736
Disease: Amyotrophic Lateral Sclerosis
485 0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 0.010 1.000 1 2012 2012
Frontotemporal Lobar Degeneration
CUI: C0751072
Disease: Frontotemporal Lobar Degeneration
54 0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 0.010 1.000 1 2009 2009
GRN-related frontotemporal dementia
CUI: C3811918
Disease: GRN-related frontotemporal dementia
20 0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 0.010 1.000 1 2009 2009
INCLUSION BODY MYOPATHY WITH EARLY-ONSET PAGET DISEASE AND FRONTOTEMPORAL DEMENTIA
6 0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 0.010 1.000 1 2009 2009
Myopathy
CUI: C0026848
Disease: Myopathy
166 0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 0.010 1.000 1 2009 2009