Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519880 0.925 0.080 19 49665875 missense variant C/T snv 4.0E-06 2
rs1057519885 0.925 0.080 20 20052443 missense variant G/A snv 2
rs137854599 0.882 0.080 9 21971093 missense variant C/G;T snv 2
rs267600971 0.882 0.080 6 31972346 missense variant G/A snv 2
rs868438023 0.882 0.080 15 40382906 missense variant C/T snv 2
rs1057519955 1.000 0.080 2 218584682 missense variant C/T snv 1
rs1805006 0.790 0.080 16 89919510 missense variant C/A;G snv 5.2E-03; 4.0E-06 1
rs267599211 0.882 0.080 2 218584683 missense variant C/T snv 1
rs121913386 0.807 0.120 9 21971018 missense variant G/A;T snv 6
rs121913512
KIT
0.851 0.120 4 54728055 missense variant A/C;G snv 6
rs1057519728 0.851 0.120 15 66435103 missense variant T/A;C;G snv 5
rs1057519757 0.882 0.120 5 68293310 missense variant G/A;C snv 5
rs1057519841 0.925 0.120 5 68295269 missense variant A/G snv 5
rs1057519874 0.807 0.120 7 6387261 missense variant C/A;T snv 4
rs1057519908 0.882 0.120 15 66435105 missense variant T/G snv 4
rs1057519948 0.851 0.120 7 6387262 missense variant C/T snv 4
rs1057519907
KIT
0.925 0.120 4 54728057 missense variant A/C snv 2
rs763733111 0.925 0.120 9 125149801 missense variant G/A snv 4.0E-06 2
rs759610249 0.790 0.160 4 152323032 missense variant C/T snv 8.0E-06 7.0E-06 8
rs1057519917 0.807 0.160 1 11124517 missense variant A/G;T snv 7
rs1057519732 0.827 0.160 15 66436824 missense variant C/A;T snv 6
rs104894104 0.790 0.160 9 21971019 missense variant G/A;T snv 4
rs1057519910 0.851 0.160 19 4117551 missense variant A/C;T snv 4
rs1057519742 0.827 0.160 19 3118944 missense variant A/C;T snv 3
rs1057519786 0.882 0.160 X 47566722 missense variant C/G;T snv 3