Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs281860566 1.000 0.080 6 31270339 missense variant C/T snv 1
rs760454379 1.000 0.080 7 50400082 missense variant G/A snv 1.6E-05 7.0E-06 1
rs12573787 1.000 0.080 10 87863959 5 prime UTR variant G/A;C snv 1
rs1257378 1.000 0.080 11 94621792 intron variant A/T snv 1
rs9610915 1.000 0.080 22 38215073 3 prime UTR variant C/G snv 0.48 0.41 1
rs754736070 1.000 0.080 4 99597206 missense variant T/C snv 8.0E-06 7.0E-06 1
rs1414109649 1.000 0.080 5 40765164 missense variant A/G snv 4.0E-06 1
rs369488601 1.000 0.080 22 23181175 missense variant G/A;C snv 1.9E-05; 9.7E-05 1
rs775014154 1.000 0.080 22 23181637 missense variant C/T snv 5.8E-05 7.0E-05 1
rs1178702025 1.000 0.080 18 44951912 missense variant G/A snv 1
rs1057519771 1.000 0.080 9 130872201 missense variant G/C snv 2
rs121913454 0.925 0.080 9 130874969 missense variant A/G snv 2
rs121913460 0.925 0.080 9 130862971 missense variant A/T snv 2
rs1314838108 0.925 0.160 9 130854977 missense variant G/A snv 7.0E-06 2
rs111340708 0.925 0.080 12 111447548 intron variant TGGGGTGGGGTGGGG/-;TGGGG;TGGGGTGGGG;TGGGGTGGGGTGGGGTGGGG;TGGGGTGGGGTGGGGTGGGGTGGGG delins 0.52 2
rs918140013 0.925 0.080 12 111447663 missense variant G/A snv 7.0E-06 2
rs121913505
KIT
0.925 0.080 4 54695598 missense variant G/A snv 2.0E-05 2
rs137852974 0.925 0.200 11 62691132 stop gained G/A snv 4.0E-06 2
rs1208076129 0.925 0.120 6 31164861 stop gained G/A snv 4.1E-06 2.1E-05 2
rs1483790387 0.925 0.120 5 115625762 missense variant C/A snv 2
rs141157255 0.882 0.120 12 98659331 missense variant G/A snv 4.0E-05 2.8E-05 3
rs3092856
ATM
0.882 0.120 11 108289005 missense variant C/T snv 1.2E-02 2.2E-02 3
rs1407906280 0.882 0.120 12 68839467 missense variant C/T snv 4.0E-06 7.0E-06 3
rs4148356 0.851 0.120 16 16083418 missense variant G/A snv 2.3E-02 1.3E-02 4
rs45511401 0.851 0.120 16 16079375 missense variant G/T snv 3.8E-02 3.6E-02 4