Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs2431689 0.882 0.040 5 160472115 intron variant G/A snv 0.17 3
rs4261436 0.925 0.040 14 32830276 3 prime UTR variant T/C snv 0.43 3
rs58064122 0.882 0.160 17 44913334 missense variant G/A;C snv 3
rs6089953 0.882 0.080 20 63659655 intron variant A/G snv 0.82 3
rs7115578 0.882 0.040 11 96266936 intron variant G/A snv 0.37 3
rs868162712 0.925 0.040 18 55279598 missense variant G/A snv 3
rs12594 0.925 0.040 1 237833787 3 prime UTR variant A/G snv 0.28 2
rs16835904 0.925 0.040 1 237833954 3 prime UTR variant C/T snv 0.17 2
rs1040177874 0.925 0.040 2 208239914 missense variant G/A snv 4.0E-06 2
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs773442580
EGF
0.851 0.080 4 109913367 missense variant T/C;G snv 4.0E-06 7
rs751857027 0.925 0.120 19 10707507 missense variant C/G;T snv 1.2E-05; 4.0E-06 2
rs779707422 0.763 0.280 8 38417331 missense variant G/A;T snv 4.0E-06 12
rs1057519897 0.807 0.240 8 38414788 missense variant C/G;T snv 4.0E-06 6
rs1476157710 0.925 0.040 12 48970460 missense variant T/C snv 4.1E-06 1.4E-05 3
rs770374782 0.851 0.160 17 7673752 missense variant G/A;C snv 1.2E-05 4.2E-05 6
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
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
rs55819519 0.627 0.400 17 7673751 missense variant C/A;G;T snv 1.6E-04 1.3E-04 40
rs118101777 0.614 0.280 15 90087472 missense variant C/T snv 2.0E-03 1.6E-03 42
rs1801516
ATM
0.627 0.400 11 108304735 missense variant G/A snv 0.11 0.11 39