Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs121913355 0.641 0.520 7 140781602 missense variant C/A;G;T snv 4.0E-06 34
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 25
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 22
rs121913255 0.667 0.400 1 114713907 missense variant T/A;G snv 19
rs121913364 0.641 0.520 7 140753334 missense variant T/C;G snv 4.0E-06 14
rs121913366 0.763 0.400 7 140753345 missense variant A/C;T snv 7
rs121913378 0.776 0.280 7 140753337 missense variant C/A;G;T snv 6
rs104894095 0.827 0.120 9 21971200 missense variant C/G;T snv 9.0E-06 3
rs121913254 0.658 0.440 1 114713909 stop gained G/A;C;T snv 3
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 2
rs993022333
KIT
0.851 0.080 4 54733173 missense variant A/C;T snv 2
rs121913227 0.653 0.320 7 140753336 missense variant AC/CT;TT mnv 1
rs121913368 0.925 0.040 7 140753345 missense variant AG/GA mnv 1
rs868224085 1.000 0.040 2 221482474 missense variant G/A snv 1
rs267601191 1.000 0.040 7 100819817 missense variant G/A snv 1
rs1451501407 1.000 0.040 17 8006628 missense variant G/A snv 1
rs1238066548 1.000 0.040 19 38595699 missense variant G/A;T snv 1
rs267601046 1.000 0.040 6 43283303 missense variant C/T snv 1
rs1057519695 0.641 0.520 1 114713907 missense variant TT/CA;CC mnv 1
rs1057519834 0.658 0.480 1 114713908 missense variant TG/CT mnv 1
rs907102077 1.000 0.040 3 9760752 missense variant G/A snv 1
rs1484691555 1.000 0.040 20 9539512 missense variant C/T snv 4.0E-06 1
rs1277219458 1.000 0.040 2 241143002 missense variant C/T snv 1
rs779173667 1.000 0.040 4 54290418 missense variant G/A snv 8.0E-06 1.4E-05 1
rs267605306 1.000 0.040 19 14446504 missense variant C/G;T snv 1.6E-05 1