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: rs1536076
rs1536076
1.000 0.040 9 17731923 intron variant T/G snv 0.19
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.800 1.000 1 2012 2012
dbSNP: rs13294100
rs13294100
1.000 0.040 9 17579692 intron variant T/G snv 0.51
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2017 2017
dbSNP: rs2209440
rs2209440
1.000 0.040 9 17736344 intron variant T/A;G snv
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.700 1.000 1 2016 2016