rs11248051, GAK

N. diseases: 2
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 864544 intron variant C/G;T snv 0.820 1.000 3 2010 2014
High density lipoprotein measurement
CUI: C0392885
Disease: High density lipoprotein measurement
1440 1.000 0.040 4 864544 intron variant C/G;T snv 0.700 1.000 1 2018 2018