Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519938 0.776 0.160 3 179203764 missense variant A/C;T snv 10
rs1057519939 0.776 0.160 3 179203763 missense variant A/C snv 10
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
rs121913284 0.776 0.160 3 179203765 missense variant T/A;G snv 11
rs759610249 0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs876660807 0.763 0.160 17 7674248 missense variant T/C snv 12
rs1057519816 0.763 0.200 17 39711955 missense variant C/A;T snv 14
rs1057519882 0.807 0.200 9 21974678 missense variant C/A snv 7
rs1057519928 0.807 0.200 3 179221147 missense variant A/C snv 8
rs1057519936 0.776 0.200 3 179234284 missense variant A/G;T snv 11
rs1057519937 0.776 0.200 3 179234285 missense variant T/C snv 11
rs1057519940 0.752 0.200 3 179218308 missense variant G/T snv 13
rs1057519884 0.752 0.240 16 3738616 missense variant C/A;T snv 11
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 17
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 19
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
rs1057519941 0.776 0.240 3 179203761 missense variant T/C;G snv 10
rs1057519989 0.732 0.240 17 7674233 missense variant C/A;G;T snv 17
rs11554273 0.689 0.240 20 58909365 missense variant C/A;G;T snv 4.0E-06 22
rs121913351 0.776 0.240 7 140781611 missense variant C/A;G;T snv 4.0E-06 9
rs397517201 0.732 0.240 3 179218307 missense variant A/C;G;T snv 16
rs587780071 0.732 0.240 17 7674951 missense variant G/A snv 15