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: rs762551
rs762551
0.701 0.400 15 74749576 intron variant C/A snv 0.67
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.040 0.500 4 2010 2018
dbSNP: rs2470890
rs2470890
0.742 0.320 15 74755085 synonymous variant T/C snv 0.57
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 < 0.001 1 2011 2011
dbSNP: rs2472304
rs2472304
1.000 0.040 15 74751897 intron variant G/A snv 0.46 0.43
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.010 1.000 1 2016 2016