Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519947 0.790 0.160 19 52212730 missense variant G/A snv 9
rs1057519999 0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs786201419 0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs876660807 0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs765848205 0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs786203071 0.776 0.240 17 7675181 missense variant T/A;G snv 8
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17
rs1057519946 0.732 0.280 19 52212729 missense variant C/G;T snv 17
rs530941076 0.695 0.280 17 7674873 missense variant A/C;G;T snv 4.0E-06 20
rs587782329 0.677 0.280 17 7674217 missense variant C/A;G;T snv 16
rs985033810 0.724 0.280 17 7674232 missense variant C/A;G;T snv 16
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
rs587780070 0.683 0.320 17 7675077 missense variant G/A;C;T snv 4.0E-06 23
rs587782664 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
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
rs876660333 0.742 0.360 17 7673805 missense variant A/C;G;T snv 13