rs201106962, SNCA

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.
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 0.010 1.000 1 2013 2013
Dementia
CUI: C0497327
Disease: Dementia
176 0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 0.020 1.000 2 2013 2014
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 0.020 1.000 2 2013 2014
PARKINSON DISEASE 1, AUTOSOMAL DOMINANT (disorder)
5 0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 0.700 1.000 7 1997 2015
Parkinson Disease
CUI: C0030567
Disease: Parkinson Disease
990 0.851 0.080 4 89828156 missense variant A/C snv 8.0E-05 7.0E-05 0.090 1.000 9 2013 2019