Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs121918464 0.708 0.440 12 112450406 missense variant G/A;C snv 25
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs281865545 0.695 0.360 17 64377836 missense variant C/G;T snv 18
rs55832599 0.716 0.360 17 7673821 missense variant G/A snv 18
rs869320694 0.742 0.520 8 38414790 missense variant T/C snv 16
rs779707422 0.763 0.280 8 38417331 missense variant G/A;T snv 4.0E-06 12
rs137852972 0.752 0.240 11 62702499 missense variant T/C snv 1.6E-05 10
rs371409680 0.790 0.120 17 7673772 missense variant C/G;T snv 4.0E-05 7.0E-06 10
rs121918465 0.827 0.200 12 112450407 missense variant A/C;G;T snv 7
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs1057519897 0.807 0.240 8 38414788 missense variant C/G;T snv 4.0E-06 6
rs770374782 0.851 0.160 17 7673752 missense variant G/A;C snv 1.2E-05 4.2E-05 6
rs1057519898 0.851 0.120 8 38417333 missense variant T/C snv 5
rs1057519899 0.851 0.120 8 38417879 missense variant T/C snv 5
rs1476157710 0.925 0.040 12 48970460 missense variant T/C snv 4.1E-06 1.4E-05 3
rs3745601 0.882 0.120 19 10113872 missense variant G/A snv 0.16 0.13 3
rs58064122 0.882 0.160 17 44913334 missense variant G/A;C snv 3
rs766727892 0.925 0.040 10 113151107 missense variant G/A snv 1.2E-05 7.0E-06 3
rs867657798 0.925 0.040 18 55631366 missense variant G/A;C snv 1.4E-05 3
rs868162712 0.925 0.040 18 55279598 missense variant G/A snv 3
rs1040177874 0.925 0.040 2 208239914 missense variant G/A snv 4.0E-06 2
rs751857027 0.925 0.120 19 10707507 missense variant C/G;T snv 1.2E-05; 4.0E-06 2
rs4809324 0.807 0.200 20 63686867 non coding transcript exon variant T/C snv 8.8E-02 7