Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs140226130 0.790 0.200 18 33336845 intron variant -/CTTTTTGCT delins 7.8E-02 8
rs10163755 0.827 0.200 18 31405413 intron variant G/A snv 0.74 6
rs10835211 1.000 0.080 11 27679818 intron variant G/A snv 0.19 3
rs2949506 0.851 0.160 18 30217168 intergenic variant C/T snv 0.14 5
rs17601696 10 121360522 intergenic variant C/T snv 6.0E-02 2
rs73956431 0.827 0.120 18 31699870 regulatory region variant C/T snv 8.4E-02 6
rs1345176461 0.716 0.240 14 77027231 stop gained G/A;T snv 4.3E-06 40
rs878853250 0.752 0.360 12 51699663 stop gained T/A;C snv 37
rs1448259271 0.790 0.240 14 77027279 stop gained C/A;T snv 23
rs1555377415 0.827 0.200 14 77027274 stop gained G/C snv 18
rs774277300 0.742 0.360 11 94447276 stop gained G/A;C;T snv 2.8E-05; 4.0E-05; 4.0E-06 17
rs912001256 0.851 0.240 17 63947062 stop gained G/A snv 17
rs149830411 0.827 0.360 17 46171276 stop gained G/A snv 5.2E-05 5.6E-05 15
rs797045283 0.827 0.320 6 157207109 stop gained C/T snv 11
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs1276519904 0.645 0.520 1 226071445 missense variant A/G snv 63
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs779027563 0.677 0.360 17 42687838 missense variant G/C snv 4.0E-06 7.0E-06 58
rs1057519389 0.695 0.400 10 129957324 missense variant C/A;G;T snv 46
rs63750687 0.752 0.200 14 73217137 missense variant C/A;G;T snv 33
rs151344517 0.742 0.320 18 12337505 missense variant C/T snv 31
rs1555968941 0.752 0.280 12 2653847 missense variant G/A;C snv 31
rs28934907 0.732 0.320 X 154032268 missense variant G/A;C snv 30
rs34757931 0.742 0.360 11 119081189 missense variant T/G snv 1.2E-04 5.6E-05 26
rs121908557 0.752 0.280 17 63957514 missense variant C/T snv 8.2E-06 1.4E-05 23