rs1768208, MOBP

N. diseases: 4
Source: ALL
Disease N. SNPs d DSI v DPI v Chr Position Consequence Alleles Class AFEXOME AFGENOME Score vda EI vda N. PMIDs First Ref. Last Ref.
Progressive supranuclear palsy
CUI: C0038868
Disease: Progressive supranuclear palsy
52 0.851 0.200 3 39481512 intron variant T/C snv 0.76 0.830 1.000 4 2011 2016
Corticobasal degeneration
CUI: C0393570
Disease: Corticobasal degeneration
14 0.851 0.200 3 39481512 intron variant T/C snv 0.76 0.700 1.000 1 2015 2015
Behavioral variant of frontotemporal dementia
10 0.851 0.200 3 39481512 intron variant T/C snv 0.76 0.010 1.000 1 2014 2014
Deuteranomaly
CUI: C3887938
Disease: Deuteranomaly
10 0.851 0.200 3 39481512 intron variant T/C snv 0.76 0.010 1.000 1 2015 2015