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: rs529974
rs529974
1.000 0.040 1 20500417 3 prime UTR variant G/A snv 0.31
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2019 2019
dbSNP: rs986952349
rs986952349
1.000 0.040 1 20507924 missense variant C/G;T snv 1.4E-05 2.8E-05
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2016 2016