Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs10012 0.716 0.280 2 38075247 missense variant G/C snv 0.31 0.36 16
rs10079250 0.827 0.120 5 150070569 missense variant T/C snv 9.9E-02 8.6E-02 7
rs1026411 0.827 0.080 8 127014165 intron variant G/A;C snv 0.25 5
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1046175 0.851 0.080 10 133391446 stop gained C/A;G;T snv 1.2E-05; 0.88 4
rs1047768 0.695 0.320 13 102852167 synonymous variant T/C snv 0.52 0.59 20
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs1048943 0.533 0.720 15 74720644 missense variant T/A;C;G snv 0.11 5.9E-02 88
rs10505477 0.658 0.400 8 127395198 intron variant A/G snv 0.40 31
rs1051753269 0.790 0.120 7 55174029 missense variant G/A snv 7.0E-06 7
rs1052133 0.476 0.800 3 9757089 missense variant C/G snv 0.27 0.22 147
rs1057519698
ALK
0.827 0.120 2 29222347 missense variant A/G;T snv 8
rs1057519729 0.827 0.080 15 66435113 missense variant A/C snv 6
rs1057519783
ALK
0.851 0.080 2 29220747 missense variant C/T snv 10
rs1057519784
ALK
0.827 0.080 2 29220765 missense variant G/T snv 7
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057519861 0.776 0.080 7 55181398 missense variant T/A snv 15
rs1057519975 0.649 0.480 17 7675209 missense variant A/C;G;T snv 34
rs10680577 0.776 0.160 19 40798690 intron variant -/TACT delins 10
rs107822 0.827 0.120 6 33207798 upstream gene variant C/T snv 0.27 0.28 5
rs10937405 0.807 0.080 3 189665394 intron variant C/T snv 0.38 9
rs1130409 0.555 0.720 14 20456995 missense variant T/A;C;G snv 4.0E-06; 4.0E-06; 0.42 72
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214