rs868435969, VCP

N. diseases: 3
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.
Cachexia
CUI: C0006625
Disease: Cachexia
11 0.925 0.280 9 35066710 missense variant G/A snv 0.010 1.000 1 2011 2011
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 0.925 0.280 9 35066710 missense variant G/A snv 0.010 1.000 1 2016 2016
Pneumonia
CUI: C0032285
Disease: Pneumonia
33 0.925 0.280 9 35066710 missense variant G/A snv 0.010 1.000 1 2011 2011