rs1801582, PRKN

N. diseases: 3
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 0.925 0.120 6 161386823 missense variant C/G;T snv 0.16; 3.2E-05 0.030 0.667 3 2003 2020
Neurologic Symptoms
CUI: C0235031
Disease: Neurologic Symptoms
30 0.925 0.120 6 161386823 missense variant C/G;T snv 0.16; 3.2E-05 0.010 1.000 1 2020 2020
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.925 0.120 6 161386823 missense variant C/G;T snv 0.16; 3.2E-05 0.010 1.000 1 2008 2008