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: rs199476135
rs199476135
0.882 0.120 MT 9176 missense variant T/C;G snv
Striatonigral Degeneration, Infantile, Mitochondrial
Nervous System Diseases 0.800 1.000 1 1995 1995
dbSNP: rs199476136
rs199476136
0.925 0.120 MT 8851 missense variant T/C snv
Striatonigral Degeneration, Infantile, Mitochondrial
Nervous System Diseases 0.700 0