rs121909331, VCP

N. diseases: 5
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
CUI: C4551951
Disease: Inclusion Body Myopathy with Early-Onset Paget Disease with or without Frontotemporal Dementia 1
9 0.851 0.200 9 35064167 missense variant G/T snv 0.800 1.000 15 2004 2018
Frontotemporal dementia
CUI: C0338451
Disease: Frontotemporal dementia
215 0.851 0.200 9 35064167 missense variant G/T snv 0.020 1.000 2 2009 2012
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.851 0.200 9 35064167 missense variant G/T snv 0.020 1.000 2 2009 2012
Myopathy
CUI: C0026848
Disease: Myopathy
166 0.851 0.200 9 35064167 missense variant G/T snv 0.010 1.000 1 2012 2012
Osteitis Deformans
CUI: C0029401
Disease: Osteitis Deformans
58 0.851 0.200 9 35064167 missense variant G/T snv 0.010 1.000 1 2012 2012