Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs28934578 0.605 0.600 17 7675088 missense variant C/A;T snv 4.0E-06 47
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs28934576 0.554 0.600 17 7673802 missense variant C/A;G;T snv 4.0E-06; 1.6E-05 78
rs755794544 0.851 0.040 7 512435 missense variant T/C snv 4.0E-06 4
rs771563543 0.851 0.040 10 31510841 missense variant G/A snv 4.0E-06 1.4E-05 5
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1320938886 0.851 0.040 1 169376605 missense variant T/G snv 4.0E-06 4
rs76151636 0.776 0.280 13 51944145 missense variant G/A;T snv 4.0E-06; 9.2E-04 10
rs2235544 0.742 0.240 1 53909897 intron variant C/A;T snv 0.53; 4.0E-06 14
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs373584770 0.827 0.120 11 105030337 missense variant G/A snv 4.0E-06 7.0E-06 5
rs4652 0.752 0.200 14 55138318 missense variant A/C snv 4.1E-06; 0.45 0.57 12
rs745542298 0.807 0.080 1 3732781 missense variant G/A;T snv 8.6E-06; 4.3E-06 2.1E-05 6
rs781490101 0.851 0.040 17 7673748 missense variant T/C snv 8.0E-06 5
rs121912438 0.605 0.520 21 31667299 missense variant G/A;C;T snv 1.2E-05; 8.0E-06 58
rs374524467 0.827 0.040 4 110632961 missense variant A/C snv 8.0E-06 7.0E-06 5
rs375391381 0.851 0.040 15 43883735 missense variant C/T snv 8.0E-06 1.4E-05 4
rs200187877 0.851 0.040 4 23795829 missense variant C/T snv 8.0E-06 7.0E-06 4
rs766265850 0.851 0.040 6 30889239 missense variant G/A snv 8.1E-06 7.0E-06 4
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs769809364 0.807 0.080 1 3732940 missense variant G/A snv 8.5E-06 1.4E-05 7
rs121913343 0.611 0.520 17 7673803 missense variant G/A;C;T snv 1.2E-05 44
rs373191257 0.827 0.080 16 56363027 missense variant T/A snv 1.6E-05 7.0E-06 5
rs371409680 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 10