Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs4880 0.500 0.840 6 159692840 missense variant A/G snv 0.48 0.47 131
rs744166 0.689 0.560 17 42362183 intron variant A/G snv 0.48 22
rs751402 0.724 0.360 13 102845848 5 prime UTR variant A/G snv 0.76 15
rs768623239 0.662 0.640 1 109689278 missense variant A/G snv 1.5E-05 26
rs7867494 0.882 0.120 9 74529284 intron variant A/G snv 0.27 6
rs876658657 0.677 0.280 3 37020356 missense variant A/G snv 4.0E-06 25
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs121913279 0.526 0.560 3 179234297 missense variant A/G;T snv 4.0E-06; 4.0E-06 101
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs1550117 0.790 0.320 2 25343038 upstream gene variant A/G;T snv 11
rs231775 0.504 0.720 2 203867991 missense variant A/G;T snv 0.42; 4.0E-06 115
rs5275 0.583 0.560 1 186673926 3 prime UTR variant A/G;T snv 55
rs397517132 0.623 0.280 7 55191846 missense variant A/T snv 48
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 31
rs12415607 0.827 0.160 10 113678445 upstream gene variant C/A snv 0.22 7
rs2736100 0.550 0.880 5 1286401 3 prime UTR variant C/A snv 0.52 83
rs751661633 0.851 0.120 22 38984136 missense variant C/A snv 4.1E-06 6
rs2267437 0.724 0.320 22 41620695 intron variant C/A;G snv 19
rs3219489 0.672 0.360 1 45331833 missense variant C/A;G snv 0.29 0.27 24
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs112445441 0.658 0.400 12 25245347 missense variant C/A;G;T snv 32
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913250 0.683 0.440 1 114716127 missense variant C/A;G;T snv 25
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 42
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96