rs542171324, SNCA

N. diseases: 6
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 0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 0.020 1.000 2 2017 2018
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 0.010 1.000 1 2018 2018
Fibrillation
CUI: C0232197
Disease: Fibrillation
8 0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 0.010 1.000 1 2018 2018
Impaired cognition
CUI: C0338656
Disease: Impaired cognition
348 0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 0.010 1.000 1 2017 2017
Mental deterioration
CUI: C0234985
Disease: Mental deterioration
121 0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 0.010 1.000 1 2017 2017
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 0.851 0.160 4 89828148 missense variant G/A;C snv 8.0E-06; 4.0E-06 0.010 1.000 1 2017 2017