Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs25487 0.441 0.800 19 43551574 missense variant T/C snv 0.68 0.71 205
rs77375493 0.458 0.760 9 5073770 missense variant G/A;T snv 3.5E-04 187
rs387907272 0.572 0.520 3 38141150 stop lost T/C snv 5.2E-05 7.0E-06 73
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs121913459 0.672 0.160 9 130872896 missense variant C/T snv 25
rs371769427 0.683 0.400 21 43104346 missense variant G/A;T snv 8.0E-06 24
rs147001633 0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04 15
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 12
rs568887534 0.807 0.240 8 30183156 missense variant A/G snv 4.0E-06 9
rs1250394819 0.807 0.240 5 115616325 missense variant C/T snv 4.0E-06 9
rs1190999960 0.807 0.240 11 65571690 missense variant G/A snv 9
rs267601394 0.807 0.200 7 148811635 missense variant T/A;G snv 8
rs397507510 0.776 0.280 12 112450361 missense variant G/A;C;T snv 8
rs377577594 0.827 0.240 2 25234374 missense variant G/A;C;T snv 1.2E-04; 8.0E-06 7
rs2239630 0.925 0.160 14 23120140 upstream gene variant A/C;G snv 6
rs9277378 0.827 0.320 6 33082502 intron variant A/G snv 0.40 5
rs373667881 0.827 0.160 8 125431222 missense variant G/A;T snv 1.1E-03 5
rs974120 0.851 0.200 8 2789080 intron variant T/C;G snv 4
rs10251201 0.851 0.160 7 7932654 intron variant T/A;C snv 4
rs9318227 0.882 0.080 13 73926833 intron variant T/A;C snv 3
rs10405859 0.882 0.080 19 45099523 intron variant T/C snv 0.48 3
rs121912472 0.925 0.080 9 5073742 missense variant G/C snv 2
rs757412228 0.925 0.080 21 34886917 missense variant C/A;T snv 4.0E-06 2
rs1483790387 0.925 0.120 5 115625762 missense variant C/A snv 2
rs1217007648 1.000 0.080 8 42306376 missense variant A/G snv 1