Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519933 0.790 0.240 3 179199156 missense variant A/G snv 11
rs1057519934 0.790 0.240 3 179199158 missense variant G/C snv 11
rs1057519935 0.790 0.240 3 179199157 missense variant A/G snv 11
rs121913228 0.742 0.200 3 41224621 missense variant T/C;G snv 11
rs1057519978 0.763 0.360 17 7675191 missense variant A/C;G;T snv 12
rs1057519999 0.763 0.160 17 7674247 missense variant T/C;G snv 12
rs765848205 0.763 0.240 17 7674253 missense variant A/C;G;T snv 12
rs876660807 0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519977 0.763 0.360 17 7675189 missense variant G/C snv 13
rs121913403 0.683 0.240 3 41224622 missense variant C/A;G;T snv 13
rs28931589 0.695 0.240 3 41224613 missense variant G/A;C;T snv 13
rs876660333 0.742 0.360 17 7673805 missense variant A/C;G;T snv 13
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs17849781 0.701 0.480 17 7673788 missense variant G/A;C;T snv 14
rs587782664 0.742 0.320 17 7674252 missense variant C/A;G;T snv 4.0E-06 14
rs867384286 0.732 0.240 4 152328233 missense variant G/A;C snv 4.3E-06 14
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 15
rs121912657 0.683 0.480 17 7673806 missense variant C/A;G;T snv 4.0E-06 15
rs17851045 0.672 0.400 12 25227341 missense variant T/A;G snv 4.0E-06 15
rs587781288 0.732 0.440 17 7675190 missense variant C/A;T snv 15
rs876659802 0.732 0.440 17 7673787 missense variant G/A;C;T snv 15
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
rs1057519747 0.716 0.280 17 7675094 missense variant A/C;G;T snv 17