Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519827 6 152011697 missense variant G/C snv 1
rs1057519854 0.882 0.080 10 121488063 missense variant A/T snv 5
rs1057519857 0.882 0.080 17 39724772 missense variant T/C snv 1
rs1057519890 0.807 0.200 17 39723966 missense variant T/A snv 7
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
rs1057519895 0.724 0.240 4 152328232 missense variant C/A;G;T snv 14
rs1057519901 0.925 0.080 10 121498525 missense variant T/G snv 5
rs1057519912 0.776 0.200 X 71129408 missense variant C/G;T snv 5
rs1057519913 0.925 0.120 1 11157172 missense variant G/C snv 3
rs1057519914 0.851 0.240 1 11157174 missense variant A/G snv 4
rs1057519915 0.851 0.160 1 11109318 missense variant A/C snv 5
rs1057519916 0.882 0.160 1 11109320 missense variant T/A snv 4
rs1057519925 0.683 0.560 3 179210291 missense variant G/A;C snv 23
rs1057519926 0.776 0.200 3 179210293 missense variant A/T snv 10
rs1057519927 0.716 0.240 3 179218295 missense variant A/C;G;T snv 18
rs1057519928 0.807 0.200 3 179221147 missense variant A/C snv 8
rs1057519929 0.776 0.320 3 179199066 missense variant G/A snv 9
rs1057519932 0.683 0.320 3 179234298 missense variant T/G snv 22
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
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