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: rs121908096
rs121908096
0.827 0.320 2 218814186 missense variant C/A;T snv 8.0E-06; 2.9E-04
CUI: C1866129
Disease: Abnormality of the cerebellum
Abnormality of the cerebellum
Nervous System Diseases 0.700 0
dbSNP: rs587778779
rs587778779
0.807 0.240 2 218814379 splice acceptor variant G/A;T snv
CUI: C1866129
Disease: Abnormality of the cerebellum
Abnormality of the cerebellum
Nervous System Diseases 0.700 0
dbSNP: rs886556800
rs886556800
0.827 0.320 2 218809576 splice acceptor variant G/T snv
CUI: C1866129
Disease: Abnormality of the cerebellum
Abnormality of the cerebellum
Nervous System Diseases 0.700 0