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: rs864309650
rs864309650
0.851 0.040 7 56104344 missense variant G/A snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.030 1.000 3 2017 2019
dbSNP: rs142444896
rs142444896
0.807 0.120 7 56106409 missense variant G/A snv 9.3E-03 7.5E-03
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2016 2016
dbSNP: rs816411
rs816411
1.000 0.040 7 56103796 intron variant C/T snv 0.53
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 < 0.001 1 2015 2015