Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs1056836 0.581 0.680 2 38071060 missense variant G/C snv 0.51 58
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs1057519865 0.742 0.240 3 138946321 missense variant G/C snv 15
rs11134527 0.677 0.400 5 168768351 intron variant G/A snv 0.25 24
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113994087
ALK
0.827 0.120 2 29209798 missense variant C/A;T snv 12
rs11655237 0.724 0.280 17 72404025 non coding transcript exon variant C/T snv 0.16 17
rs1190999960 0.807 0.240 11 65571690 missense variant G/A snv 9
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121908568 0.807 0.160 17 65536495 stop gained G/A snv 9
rs121912660 0.683 0.240 17 7673781 missense variant C/A;G;T snv 26
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs1259653415 1.000 0.080 3 196071416 missense variant T/C snv 7.0E-06 3
rs12826786 0.683 0.480 12 53961717 upstream gene variant C/T snv 0.38 26
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs1285136498 0.807 0.080 5 143400101 missense variant G/A snv 13
rs132770 0.752 0.320 22 41621260 5 prime UTR variant A/G snv 0.83 14
rs132793 0.851 0.160 22 41667677 downstream gene variant A/C;G;T snv 7
rs13281615 0.716 0.360 8 127343372 intron variant A/G snv 0.43 18
rs13428812 0.827 0.120 2 25269598 intron variant A/G snv 0.31 9
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36