Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519889 0.807 0.200 22 41169525 missense variant G/A;T snv 6
rs1057519923 0.807 0.200 2 177234081 missense variant T/A snv 6
rs1057519924 0.807 0.200 2 177234080 missense variant C/A snv 6
rs1057519920 0.790 0.160 2 177234232 missense variant C/A;G;T snv 7
rs1057519922 0.790 0.200 2 177234082 missense variant C/G;T snv 7
rs1057519881 0.776 0.240 9 21971111 missense variant T/C snv 8
rs1057519928 0.807 0.200 3 179221147 missense variant A/C snv 8
rs759610249 0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs786201419 0.790 0.160 17 7675180 missense variant C/A;T snv 8
rs121913385 0.763 0.240 9 21971112 missense variant G/A;C snv 9
rs34968276 0.776 0.240 9 21971110 stop gained G/A;C;T snv 9
rs786203071 0.776 0.240 17 7675181 missense variant T/A;G snv 9
rs1057519911 0.776 0.160 22 21772875 missense variant C/T snv 10
rs1057519921 0.763 0.240 2 177234231 missense variant T/C snv 10
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs867262025 0.790 0.360 3 179221146 missense variant G/A snv 10
rs1057519884 0.752 0.240 16 3738616 missense variant C/A;T snv 11
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
rs397516896 0.763 0.360 7 140753355 missense variant C/G;T snv 11
rs1057519896 0.742 0.320 4 152326136 missense variant C/A;T snv 12
rs121913287 0.752 0.400 3 179199088 missense variant G/A snv 12
rs398124146 0.742 0.360 16 3738617 missense variant G/A;C snv 12
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