Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7121 0.882 0.160 20 58903752 missense variant C/G;T snv 0.54 6
rs1284806277
MOK
0.827 0.200 14 102251978 missense variant A/G snv 1.4E-05 13
rs4987188 0.790 0.200 2 47416318 missense variant G/A;T snv 1.3E-02; 2.0E-05 11
rs587782529 0.851 0.200 17 7670700 missense variant G/A;C snv 8
rs4444235 0.701 0.240 14 53944201 downstream gene variant T/C snv 0.43 23
rs17217772 0.790 0.240 2 47410107 missense variant A/C;G;T snv 5.8E-03 10
rs1057519710
KIT
0.695 0.280 4 54733166 missense variant G/C;T snv 22
rs11568818 0.763 0.280 11 102530930 upstream gene variant T/A;C snv 15
rs104893626 0.827 0.280 2 136114915 stop gained G/C snv 11
rs773862672 0.882 0.280 1 11247922 missense variant G/A;C snv 1.2E-05 6
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs145204276 0.658 0.320 1 173868254 splice donor variant CAAGG/- delins 8.8E-02 31
rs375874539 0.732 0.320 17 7674237 missense variant G/A;C snv 15
rs2273535 0.645 0.360 20 56386485 missense variant A/C;T snv 0.28 38
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16
rs11549467 0.653 0.400 14 61740857 missense variant G/A snv 8.9E-03 7.0E-03 30
rs727503094 0.633 0.440 11 534287 missense variant GC/AG;AT;TA;TT mnv 41
rs9282861 0.658 0.440 16 28606193 missense variant C/T snv 31
rs1042028 0.658 0.440 16 28606193 missense variant C/T snv 0.22 0.30 30
rs752021744 0.689 0.440 3 138759306 missense variant T/C snv 1.2E-05 29
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs2057482 0.701 0.440 14 61747130 3 prime UTR variant T/C snv 0.84 0.80 21
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs2227983 0.658 0.520 7 55161562 missense variant G/A;C;T snv 0.29 31
rs869320694 0.742 0.520 8 38414790 missense variant T/C snv 16