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: rs10797576
rs10797576
1.000 0.040 1 232528865 intron variant C/T snv 0.12
CUI: C0030567
Disease: Parkinson Disease
Parkinson Disease
Nervous System Diseases 0.730 1.000 5 2014 2018