Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121918799 0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 14
rs61738009 0.827 0.080 8 67483807 stop gained C/A;T snv 4.0E-06; 2.0E-03 2.5E-03 11
rs74315442 0.851 0.200 21 43774297 stop gained G/A snv 4.0E-05 2.1E-05 10
rs35993949 0.882 0.040 8 67506804 missense variant G/C snv 1.5E-03 1.2E-03 9
rs765965968 0.882 0.080 16 2498333 missense variant G/A;T snv 1.3E-05; 4.2E-06 5
rs397514737 0.882 0.080 5 162149153 missense variant G/A snv 4
rs118192247 0.882 0.080 8 132175491 missense variant C/T snv 3
rs121918817 0.882 0.040 2 166045080 missense variant C/T snv 1.7E-03 1.5E-03 3
rs1250662891 0.925 0.040 16 10180176 missense variant G/C snv 4.0E-06 2
rs1264858438 0.925 0.080 20 63406931 missense variant C/T snv 9.0E-06 1.4E-05 2
rs1555482933 0.925 0.040 16 9764834 missense variant T/A snv 2
rs1555488144 0.925 0.040 16 9798454 missense variant C/T snv 2
rs1555491648 0.925 0.040 16 9822337 missense variant G/A snv 2
rs1555496111 0.925 0.040 16 9849778 missense variant A/G snv 2
rs201868078 0.925 0.040 20 63408524 missense variant G/A;C snv 1.6E-05 2
rs397518465 0.925 0.040 16 9937958 splice donor variant C/A;T snv 2
rs768456731 0.925 0.040 22 31765049 missense variant G/A;T snv 1.6E-05 2
rs779989663 0.925 0.040 16 9841092 missense variant A/T snv 4.8E-05 7.0E-06 2
rs114684479 1.000 0.040 7 103596518 missense variant G/T snv 1.6E-03 1.4E-03 1
rs115035120 1.000 0.040 7 103483741 missense variant C/T snv 8.5E-04 2.9E-04 1
rs1238779318 1.000 0.040 16 9938274 missense variant C/G;T snv 1
rs1306918506 1.000 0.040 1 43439950 missense variant A/T snv 8.0E-06 1
rs1381851622 1.000 0.040 8 132174283 missense variant C/T snv 1.9E-05 1
rs138282349 1.000 0.040 9 135792094 missense variant G/A snv 1.0E-03 1.2E-03 1
rs1383795440 1.000 0.040 22 31754865 5 prime UTR variant G/C snv 7.0E-06 1