Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs781049584
APP
0.724 0.280 21 26021917 missense variant T/G snv 8.2E-06 7.0E-06 18
rs387906789
VCP
0.742 0.200 9 35065352 missense variant G/A;C snv 4.0E-06 14
rs121909330
VCP
0.752 0.200 9 35065364 missense variant G/A;C;T snv 11
rs121909334
VCP
0.752 0.200 9 35065255 missense variant C/T snv 1.6E-05 10
rs121909335
VCP
0.776 0.200 9 35065351 missense variant C/T snv 8.0E-06 9
rs121909331
VCP
0.851 0.200 9 35064167 missense variant G/T snv 5