Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1801394 0.531 0.840 5 7870860 missense variant A/G snv 0.47 0.45 101
rs121913488 0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs1057519766 0.851 0.080 13 28028203 missense variant G/C;T snv 5
rs35602083 0.851 0.040 13 28049450 missense variant C/T snv 1.7E-02 1.6E-02 4
rs753000469 0.851 0.200 1 212859113 missense variant C/T snv 4.0E-06 4
rs4925 0.677 0.560 10 104263031 missense variant C/A snv 0.25 0.23 28
rs1695 0.457 0.880 11 67585218 missense variant A/G snv 0.34 0.36 188
rs1275561861 0.672 0.360 6 29944350 missense variant G/A snv 23
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs104894230 0.564 0.600 11 534288 missense variant C/A;G;T snv 73
rs121913502 0.708 0.320 15 90088702 missense variant C/A;T snv 3.2E-05 19
rs6964823 0.925 0.040 7 50392398 intron variant G/A snv 0.45 3
rs2243250
IL4
0.570 0.760 5 132673462 upstream gene variant C/T snv 0.35 61
rs2070874
IL4
0.672 0.560 5 132674018 5 prime UTR variant C/T snv 0.28 0.28 27
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs1057519753 0.763 0.120 1 64846664 missense variant C/A snv 9
rs869312953 0.851 0.120 1 64846735 missense variant G/T snv 5
rs121913682
KIT
0.605 0.400 4 54733167 missense variant A/G;T snv 52
rs121913507
KIT
0.614 0.400 4 54733155 missense variant A/T snv 49
rs3822214
KIT
0.732 0.240 4 54727298 missense variant A/C;G;T snv 7.7E-02; 8.0E-06 13
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 12
rs121913521
KIT
0.790 0.120 4 54727447 missense variant T/A;C;G snv 12
rs861539 0.519 0.680 14 103699416 missense variant G/A snv 0.29 0.30 104
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs9318227 0.882 0.080 13 73926833 intron variant T/A;C snv 3