rs1060501198, TP53

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 0.925 0.040 17 7674900 missense variant T/C;G snv 0.020 1.000 2 2006 2010
Mitochondrial abnormalities
CUI: C4020732
Disease: Mitochondrial abnormalities
20 0.925 0.040 17 7674900 missense variant T/C;G snv 0.010 1.000 1 2007 2007
Movement Disorders
CUI: C0026650
Disease: Movement Disorders
247 0.925 0.040 17 7674900 missense variant T/C;G snv 0.010 1.000 1 2006 2006