rs4752293, GRK5

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 0.882 0.080 10 119342186 intron variant C/T snv 0.74 0.020 1.000 2 2011 2015
Dementia
CUI: C0497327
Disease: Dementia
176 0.882 0.080 10 119342186 intron variant C/T snv 0.74 0.010 1.000 1 2015 2015
Presenile dementia
CUI: C0011265
Disease: Presenile dementia
159 0.882 0.080 10 119342186 intron variant C/T snv 0.74 0.010 1.000 1 2015 2015