rs1994090, SLC2A13

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 12 40034759 intron variant G/A;T snv 0.810 1.000 4 2009 2016
Prion Diseases
CUI: C0162534
Disease: Prion Diseases
67 1.000 0.040 12 40034759 intron variant G/A;T snv 0.700 1.000 1 2012 2012