rs1801334, PRKN

N. diseases: 4
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 0.851 0.040 6 161360193 missense variant C/T snv 2.5E-02 2.5E-02 0.020 1.000 2 2002 2010
Familial (FPAH)
CUI: C1611743
Disease: Familial (FPAH)
276 0.851 0.040 6 161360193 missense variant C/T snv 2.5E-02 2.5E-02 0.010 1.000 1 2003 2003
Sporadic Parkinson disease
CUI: C4511452
Disease: Sporadic Parkinson disease
65 0.851 0.040 6 161360193 missense variant C/T snv 2.5E-02 2.5E-02 0.010 1.000 1 2005 2005
Young onset Parkinson disease
CUI: C4275179
Disease: Young onset Parkinson disease
32 0.851 0.040 6 161360193 missense variant C/T snv 2.5E-02 2.5E-02 0.010 1.000 1 2003 2003