Disease: Corticobasal degeneration
Source: ALL
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs143624519
MAPT
0.724 0.240 17 45991484 missense variant G/A;T snv 1.5E-03; 1.2E-05 17
rs242557
MAPT
0.752 0.200 17 45942346 intron variant G/A snv 0.36 12
rs76980269
NOS1
0.763 0.280 12 117330794 synonymous variant G/A snv 2.8E-05 4.2E-05 10
rs1768208
MOBP
0.851 0.200 3 39481512 intron variant T/C snv 0.76 4