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: rs786205232
rs786205232
0.925 0.040 1 110603893 missense variant C/T snv 4.0E-06
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
Nervous System Diseases 0.700 1.000 28 1991 2017
dbSNP: rs886041761
rs886041761
0.925 0.200 1 110603902 missense variant C/T snv
CUI: C0026650
Disease: Movement Disorders
Movement Disorders
Nervous System Diseases 0.700 1.000 28 1991 2017