Source: BEFREE

Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
0.776 0.240 4 89716450 intron variant G/A snv 0.54
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease 		0.900 1.000 15 2008 2019
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
0.776 0.240 4 89716450 intron variant G/A snv 0.54
CUI: C4511452
Disease: Sporadic Parkinson disease
Sporadic Parkinson disease 		0.020 1.000 2 2013 2017
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
0.776 0.240 4 89716450 intron variant G/A snv 0.54
CUI: C0002395
Disease: Alzheimer's Disease
Alzheimer's Disease 		0.010 1.000 1 2018 2018
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
0.776 0.240 4 89716450 intron variant G/A snv 0.54
CUI: C0017205
Disease: Gaucher Disease
Gaucher Disease 		0.010 1.000 1 2014 2014
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
0.776 0.240 4 89716450 intron variant G/A snv 0.54
CUI: C0003467
Disease: Anxiety
Anxiety 		0.010 1.000 1 2018 2018
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
0.776 0.240 4 89716450 intron variant G/A snv 0.54
CUI: C0001956
Disease: Alcohol Use Disorder
Alcohol Use Disorder 		0.010 1.000 1 2018 2018
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
0.776 0.240 4 89716450 intron variant G/A snv 0.54
CUI: C0338656
Disease: Impaired cognition
Impaired cognition 		0.010 1.000 1 2017 2017
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
0.776 0.240 4 89716450 intron variant G/A snv 0.54
CUI: C0003469
Disease: Anxiety Disorders
Anxiety Disorders 		0.010 1.000 1 2018 2018
dbSNP: rs356219
rs356219
SNCA ; LOC105377329
0.776 0.240 4 89716450 intron variant G/A snv 0.54
CUI: C0751772
Disease: REM Sleep Behavior Disorder
REM Sleep Behavior Disorder 		0.010 1.000 1 2018 2018