rs12817488, CCDC62

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 12 122811747 intron variant G/A snv 0.39 0.850 0.857 7 2011 2016
Prion Diseases
CUI: C0162534
Disease: Prion Diseases
67 1.000 0.040 12 122811747 intron variant G/A snv 0.39 0.700 1.000 1 2012 2012
Parkinsonian Disorders
CUI: C0242422
Disease: Parkinsonian Disorders
95 1.000 0.040 12 122811747 intron variant G/A snv 0.39 0.010 1.000 1 2014 2014