Variant DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Disease Disease Class Score vda EI vda N. PMIDs First Ref. Last Ref.
dbSNP: rs2958720
rs2958720
1.000 0.040 15 78466335 missense variant C/G snv 2.8E-02
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 < 0.001 1 2002 2002
dbSNP: rs376011164
rs376011164
1.000 0.040 15 78471857 missense variant C/G snv 4.4E-05 7.7E-05
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2002 2002