Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs587777893 0.658 0.240 1 11128107 missense variant G/A;T snv 67
rs1554333853 0.689 0.320 7 40046006 missense variant A/G snv 54
rs752298579 0.701 0.480 22 20061538 missense variant G/A snv 1.4E-04 7.0E-06 48
rs1057519389 0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs1556425596 0.752 0.240 21 45989967 intron variant C/T snv 37
rs1043679457 0.752 0.400 5 60927745 intron variant C/A;G;T snv 33
rs559979281 0.742 0.440 2 121530892 non coding transcript exon variant C/G;T snv 7.7E-06; 2.3E-05; 3.5E-04 23
rs863225422 0.742 0.440 2 121530927 non coding transcript exon variant G/A snv 4.6E-05; 7.7E-06 4.9E-05 23
rs138659167 0.807 0.320 11 71435840 splice acceptor variant C/A;G snv 5.6E-05; 3.9E-03 20
rs1032242817 0.807 0.320 11 71441307 stop gained C/T snv 8.0E-06 7.0E-06 17
rs1554603293 0.752 0.320 8 60849154 missense variant G/A snv 17
rs797045412 0.776 0.280 9 92718565 missense variant G/A;T snv 17
rs758361736 0.776 0.240 15 89649836 missense variant T/G snv 1.3E-05 1.4E-05 16
rs267607093 0.851 0.160 4 55359444 stop gained G/A snv 4.0E-06 14
rs397515415 0.807 0.240 X 72495216 stop gained G/A;T snv 10
rs1554823375 0.851 0.160 10 1080454 missense variant C/T snv 8
rs431905509 0.807 0.280 22 19176222 missense variant G/A;C snv 2.0E-05 8
rs1057518921 1.000 X 71132465 missense variant G/A snv 7
rs1565977796 0.882 0.120 13 26337623 stop gained C/A snv 7
rs542652468 0.882 19 41986177 missense variant G/A;T snv 6
rs1085308053 0.882 0.080 10 87952230 missense variant C/T snv 5
rs1569234334 0.851 0.200 X 70329420 missense variant G/T snv 5
rs564185858 0.882 0.040 10 110122249 missense variant G/A snv 1.2E-05 1.4E-05 4
rs121912708 1.000 0.040 5 126583997 stop gained G/A;C snv 6.0E-05; 4.0E-06 3
rs140845195 1.000 0.040 5 126545020 splice acceptor variant C/A;T snv 1.6E-05; 4.0E-06 3