rs104893877, SNCA

N. diseases: 59
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.
Mitochondrial abnormalities
CUI: C4020732
Disease: Mitochondrial abnormalities
20 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2007 2007
Multiple Chronic Conditions
CUI: C3266262
Disease: Multiple Chronic Conditions
42 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2016 2016
Pick Disease of the Brain
CUI: C0236642
Disease: Pick Disease of the Brain
83 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1 2017 2017
Progressive cGVHD
CUI: C3539781
Disease: Progressive cGVHD
40 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2008 2008
Progressive Neoplastic Disease
CUI: C0677932
Disease: Progressive Neoplastic Disease
40 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2008 2008
Secondary Parkinson Disease
CUI: C0030569
Disease: Secondary Parkinson Disease
1 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2008 2008
Sleep disturbances
CUI: C0037317
Disease: Sleep disturbances
74 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2013 2013
Varicosity
CUI: C0042345
Disease: Varicosity
51 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2017 2017
[D]Sleep disturbances (& [hypersomnia] or [insomnia])
CUI: C0947785
Disease: [D]Sleep disturbances (& [hypersomnia] or [insomnia])
23 0.614 0.360 4 89828149 missense variant C/T snv 0.010 1.000 1 2013 2013