rs894278, SNCA

N. diseases: 4
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.
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.882 0.080 4 89813384 intron variant T/G snv 0.15 0.720 1.000 5 2009 2019
PARKINSON DISEASE, LATE-ONSET
CUI: C3160718
Disease: PARKINSON DISEASE, LATE-ONSET
76 0.882 0.080 4 89813384 intron variant T/G snv 0.15 0.010 1.000 1 2017 2017
REM Sleep Behavior Disorder
CUI: C0751772
Disease: REM Sleep Behavior Disorder
16 0.882 0.080 4 89813384 intron variant T/G snv 0.15 0.010 1.000 1 2017 2017
Sense of smell impaired
CUI: C2364082
Disease: Sense of smell impaired
12 0.882 0.080 4 89813384 intron variant T/G snv 0.15 0.010 1.000 1 2017 2017