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: rs1768208
rs1768208
0.851 0.200 3 39481512 intron variant T/C snv 0.76
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases 0.830 1.000 4 2011 2016
dbSNP: rs10675541
rs10675541
1.000 0.120 3 39468795 intron variant -/CA delins
CUI: C0038868
Disease: Progressive supranuclear palsy
Progressive supranuclear palsy
Pathological Conditions, Signs and Symptoms; Eye Diseases; Nervous System Diseases 0.700 1.000 1 2018 2018