Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs28934575 0.641 0.400 17 7674230 missense variant C/A;G;T snv 37
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs587778720 0.667 0.360 17 7674893 missense variant C/A;G;T snv 4.0E-06 31
rs1057519945 0.776 0.200 12 132673703 missense variant C/A;T snv 12
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs2010963 0.542 0.840 6 43770613 5 prime UTR variant C/G snv 0.68 82
rs121909224 0.627 0.560 10 87933147 stop gained C/G;T snv 1.2E-05 41
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs10069690 0.595 0.560 5 1279675 intron variant C/T snv 0.36 53
rs118101777 0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs16906252 0.732 0.200 10 129467281 synonymous variant C/T snv 5.5E-02 5.1E-02 19
rs2736098 0.600 0.600 5 1293971 synonymous variant C/T snv 0.29 0.22 48
rs3856806 0.637 0.440 3 12434058 synonymous variant C/T snv 0.13 0.11 41
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs1800734 0.653 0.400 3 36993455 5 prime UTR variant G/A snv 0.22 30
rs1801133 0.472 0.880 1 11796321 missense variant G/A snv 0.31 0.27 174
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs104886003 0.562 0.440 3 179218303 missense variant G/A;C snv 4.0E-06 71
rs121912651 0.605 0.680 17 7674221 missense variant G/A;C snv 4.0E-06 53
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs28934574 0.658 0.440 17 7673776 missense variant G/A;C snv 4.0E-06 31
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44