Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs34637584 0.583 0.480 12 40340400 missense variant G/A snv 5.3E-04 3.6E-04 78
rs429358 0.590 0.600 19 44908684 missense variant T/C snv 0.14 0.16 66
rs11136000
CLU
0.752 0.160 8 27607002 intron variant T/C snv 0.56 19
rs1223904774
APP
0.790 0.120 21 25891772 missense variant C/T snv 4.0E-06 7.0E-06 8