rs11158026, GCH1

N. diseases: 1
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 14 54882151 intron variant C/A;G;T snv 0.730 1.000 6 2014 2018