Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519891 0.851 0.160 12 56088557 missense variant G/A;T snv 4.0E-06 5
rs1057519892 0.851 0.160 12 56088558 missense variant A/T snv 5
rs1057519893 0.790 0.160 12 56085070 missense variant G/A;T snv 8
rs1057519931 0.827 0.160 3 179199141 missense variant G/C snv 6
rs759610249 0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 18
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 14
rs747241612 0.752 0.240 4 152326215 missense variant G/C snv 4.0E-06 12
rs866987936 0.752 0.240 4 152326214 missense variant C/A;G;T snv 12
rs121913286 0.677 0.280 3 179218306 missense variant C/A;G snv 20
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs753660142 0.708 0.280 17 7673782 missense variant T/C;G snv 1.6E-05 19
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
rs121913274 0.645 0.320 3 179218304 missense variant A/C;G;T snv 28
rs121913275 0.672 0.320 3 179218305 missense variant G/A;C;T snv 4.0E-06 25
rs149680468 0.742 0.320 4 152326137 missense variant G/A;C;T snv 12
rs375874539 0.732 0.320 17 7674237 missense variant G/A;C snv 11
rs1057519996 0.701 0.360 17 7675217 splice acceptor variant T/A;C;G snv 16
rs1057520002 0.695 0.360 17 7674242 missense variant A/C;G snv 20
rs121912666 0.645 0.360 17 7674872 missense variant T/C;G snv 8.0E-06 24
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 25
rs121912655 0.724 0.400 17 7674238 missense variant C/A;G;T snv 15
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 11