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
rs63750231 0.689 0.160 14 73198100 missense variant A/C;G snv 23
rs121918100
TTR
0.827 0.160 18 31595184 missense variant T/C snv 11
rs17070145 0.790 0.120 5 168418786 intron variant C/T snv 0.43 10
rs63751039
APP
0.776 0.200 21 25891855 missense variant T/C snv 8
rs529782627
APP
0.882 0.120 21 26112051 missense variant C/A snv 4.0E-06 7.0E-06 3