Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1034749666 0.776 0.160 21 33027257 missense variant G/A snv 9
rs1042522 0.426 0.800 17 7676154 missense variant G/C;T snv 0.67 242
rs1045485 0.637 0.480 2 201284866 missense variant G/A;C;T snv 4.0E-06; 9.0E-02 34
rs1045642 0.456 0.840 7 87509329 synonymous variant A/G;T snv 0.50 214
rs1057519902 0.742 0.160 1 226064451 missense variant G/C snv 16
rs1057519903 0.683 0.080 1 226064434 missense variant A/T snv 28
rs1131691014 0.439 0.800 17 7676154 frameshift variant -/C ins 214
rs113488022 0.351 0.840 7 140753336 missense variant A/C;G;T snv 4.0E-06 490
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913499 0.605 0.520 2 208248389 missense variant G/A;C;T snv 51
rs121913500 0.529 0.600 2 208248388 missense variant C/A;G;T snv 4.0E-06 96
rs1273593548 0.716 0.160 7 106867593 missense variant T/G snv 8.4E-06 19
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs1353702185 0.550 0.720 12 68839311 missense variant C/G snv 4.0E-06 79
rs1385943435 0.851 0.040 9 37002662 missense variant C/A;G;T snv 4.1E-06; 4.1E-06 5
rs1444669684 0.658 0.480 9 21994285 missense variant C/A;T snv 36
rs1553260624 0.763 0.080 1 226064454 missense variant G/A snv 14
rs17006625 0.925 0.080 3 20119604 missense variant A/C;G snv 4.0E-06; 3.3E-02 3
rs1799793 0.557 0.640 19 45364001 missense variant C/A;T snv 7.1E-06; 0.29 72
rs1800371 0.742 0.240 17 7676230 missense variant G/A;T snv 1.2E-03 15
rs1800925 0.627 0.560 5 132657117 non coding transcript exon variant C/G;T snv 37
rs2279115 0.724 0.320 18 63319604 5 prime UTR variant G/A;T snv 18
rs2305948
KDR
0.732 0.400 4 55113391 missense variant C/A;T snv 4.0E-06; 0.11 18
rs2536512 0.752 0.280 4 24799693 missense variant G/A;T snv 0.55 14
rs25489 0.550 0.720 19 43552260 missense variant C/G;T snv 8.5E-06; 7.1E-02 78