Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs138817062
PML
0.882 0.040 15 74044940 missense variant C/T snv 4.0E-05 7.0E-06 4
rs35602083 0.851 0.040 13 28049450 missense variant C/T snv 1.7E-02 1.6E-02 4
rs1057519766 0.851 0.080 13 28028203 missense variant G/C;T snv 5
rs556915505 0.851 0.080 3 169143780 missense variant T/C snv 4.0E-06 7.0E-06 5
rs74315450 0.851 0.120 21 34859485 missense variant C/T snv 5
rs11545078
GGH
0.807 0.200 8 63026205 missense variant G/A snv 8.8E-02 7.8E-02 6
rs1408538785 0.827 0.080 6 38761760 missense variant A/G snv 7.0E-06 6
rs387906553 0.827 0.120 19 853022 missense variant G/A;C snv 1.2E-05 6
rs121913488 0.807 0.120 13 28018505 missense variant C/A;G;T snv 7
rs762613037 0.790 0.160 21 45512196 missense variant A/G snv 2.1E-05 7.0E-06 7
rs869312828 0.807 0.080 5 177512369 missense variant C/T snv 7
rs1482518887 0.790 0.040 21 34887018 missense variant C/T snv 7.0E-06 8
rs1057519753 0.763 0.120 1 64846664 missense variant C/A snv 9
rs2293157 0.763 0.120 17 42300657 intron variant C/A;T snv 9
rs778036161 0.776 0.080 8 92017363 missense variant T/C snv 8.0E-06 9
rs1470755915 0.776 0.240 8 92005229 missense variant C/A snv 7.0E-06 10
rs927698341 0.776 0.240 8 92005280 synonymous variant C/A snv 4.0E-06 2.8E-05 10
rs10821936 0.742 0.200 10 61963818 intron variant C/T snv 0.69 11
rs121913514
KIT
0.763 0.240 4 54733174 missense variant T/A;G snv 12
rs121913521
KIT
0.790 0.120 4 54727447 missense variant T/A;C;G snv 12
rs796065343 0.776 0.080 1 36467833 missense variant G/A snv 12
rs3822214
KIT
0.732 0.240 4 54727298 missense variant A/C;G;T snv 7.7E-02; 8.0E-06 13
rs2228014 0.752 0.240 2 136115514 synonymous variant G/A snv 4.6E-02 3.5E-02 14
rs147001633 0.776 0.240 2 25234373 missense variant C/A;G;T snv 4.0E-06; 4.0E-06; 2.2E-04 15
rs562015640 0.742 0.360 10 87960957 stop gained A/G;T snv 1.2E-05 16