Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1217691063 0.330 0.920 1 11796309 missense variant A/G snv 4.0E-06 7.0E-06 614
rs6265 0.436 0.760 11 27658369 missense variant C/T snv 0.19 0.15 272
rs4680 0.442 0.920 22 19963748 missense variant G/A snv 0.46 0.44 249
rs759834365 0.448 0.760 11 27658456 missense variant C/T snv 1.2E-05 237
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs25531 0.581 0.520 17 30237328 upstream gene variant T/C snv 0.18 72
rs6311 0.645 0.640 13 46897343 upstream gene variant C/T snv 0.40 41
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs28934908 0.732 0.280 X 154031409 missense variant G/A;T snv 5.5E-06 23
rs6314 0.677 0.360 13 46834899 missense variant G/A snv 7.9E-02 9.5E-02 23
rs893924483 0.716 0.280 11 27658285 missense variant C/A;T snv 4.0E-06 1.4E-05 23
rs121918799 0.752 0.120 2 166015636 missense variant G/C snv 1.7E-03 1.6E-03 14
rs121917893 0.807 0.160 X 71167508 missense variant C/T snv 10
rs397514679 0.790 0.200 X 47574321 stop gained G/A snv 9
rs301430 0.827 0.080 9 4576680 synonymous variant T/C snv 0.36 0.38 7
rs6323 0.807 0.040 X 43731789 synonymous variant G/T snv 0.65 7
rs2168351 0.851 0.120 15 92440492 intron variant A/G snv 0.33 6
rs3784730 0.851 0.120 15 92443898 intron variant A/G snv 0.44 6
rs141441277 0.882 0.120 X 100689933 missense variant G/A snv 5.6E-04 3.8E-04 5
rs2279357 0.851 0.160 15 74338282 intron variant T/C snv 0.69 5
rs4307059 0.882 0.080 5 25967594 intron variant T/A;C snv 5
rs779545541 0.882 0.120 14 66965293 missense variant C/T snv 4.0E-06 5
rs1858830
MET
0.925 0.040 7 116672385 5 prime UTR variant C/G snv 0.40 4
rs6551665 0.882 0.040 4 61873823 intron variant G/A snv 0.59 4
rs201551401 0.925 0.040 7 124746694 missense variant C/T snv 6.4E-05 1.4E-05 3