Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2071203 0.827 0.120 3 50274469 missense variant C/T snv 0.12 9.9E-02 6
rs680055 0.851 0.120 7 99859982 missense variant C/A;G snv 6.5E-02 0.13 5
rs7463708 0.807 0.120 8 127091810 non coding transcript exon variant G/T snv 0.27 7
rs7837328 0.882 0.120 8 127410882 intron variant A/G snv 0.52 8
rs7965399 0.851 0.120 12 102497908 regulatory region variant T/A;C snv 5
rs10090154 0.807 0.160 8 127519892 intergenic variant T/A;C snv 7
rs1012477 0.827 0.160 1 7798075 intron variant G/C snv 0.16 8
rs1042489 0.851 0.160 17 78224125 3 prime UTR variant T/C snv 0.40 5
rs1290923018 0.851 0.160 11 65570699 missense variant G/A snv 4.0E-06 5
rs1512268 0.851 0.160 8 23668950 intergenic variant T/C snv 0.50 6
rs16901946 0.827 0.160 8 127088680 non coding transcript exon variant A/G snv 1.7E-02 8
rs1801320 0.742 0.160 15 40695330 5 prime UTR variant G/C snv 0.12 15
rs1801321 0.790 0.160 15 40695367 5 prime UTR variant G/C;T snv 0.35 8
rs1859962 0.882 0.160 17 71112612 intron variant G/T snv 0.56 4
rs2735839 0.827 0.160 19 50861367 upstream gene variant A/C;G snv 7
rs4792311 0.776 0.160 17 13011692 missense variant G/A;C snv 0.27 9
rs565453 0.882 0.160 5 112849696 intron variant A/C;G snv 4
rs605059 0.763 0.160 17 42554888 missense variant G/A;C;T snv 0.56; 9.0E-05; 1.4E-05 15
rs12338 0.807 0.200 8 11853379 missense variant G/A;C;T snv 8.0E-06; 0.38; 2.4E-05 10
rs3774262 0.851 0.200 3 186854025 intron variant G/A snv 0.10 5
rs864622007
AR
0.882 0.200 X 67711621 missense variant T/A snv 5
rs138213197 0.701 0.240 17 48728343 missense variant C/T snv 1.8E-03 1.6E-03 24
rs28366003 0.763 0.240 16 56608579 upstream gene variant A/C;G snv 4.6E-02 10
rs3822214
KIT
0.732 0.240 4 54727298 missense variant A/C;G;T snv 7.7E-02; 8.0E-06 13
rs4988483 0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11