rs1564282, GAK

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 1.000 0.040 4 858525 intron variant C/T snv 8.1E-02 0.870 0.889 9 2009 2015
Triglycerides measurement
CUI: C0202236
Disease: Triglycerides measurement
1418 1.000 0.040 4 858525 intron variant C/T snv 8.1E-02 0.700 1.000 1 2018 2018
Tremor
CUI: C0040822
Disease: Tremor
52 1.000 0.040 4 858525 intron variant C/T snv 8.1E-02 0.010 1.000 1 2014 2014