Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs1057519788 0.925 0.080 6 117317184 missense variant C/T snv 6
rs1057519847 0.570 0.560 7 55191821 missense variant CT/AG mnv 72
rs1057519848 0.570 0.560 7 55191822 missense variant TG/GT mnv 72
rs11554290 0.583 0.600 1 114713908 missense variant T/A;C;G snv 59
rs121434568 0.568 0.560 7 55191822 missense variant T/A;G snv 73
rs121913377 0.354 0.840 7 140753335 missense variant CA/AT;TT mnv 480
rs121913430 1.000 0.080 7 55174740 missense variant G/A snv 3
rs1982073 0.649 0.640 19 41353016 missense variant G/A;C snv 32
rs2279744 0.605 0.640 12 68808800 intron variant T/G snv 0.31 48
rs3021094 0.827 0.360 1 206771607 intron variant T/G snv 8.0E-02 8
rs3761548 0.620 0.680 X 49261784 intron variant G/A;T snv 42
rs772092699 0.925 0.080 1 22912497 missense variant C/A;G;T snv 4.0E-06 3
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
rs13181 0.487 0.760 19 45351661 stop gained T/A;G snv 4.0E-06; 0.32 134
rs121913529 0.492 0.680 12 25245350 missense variant C/A;G;T snv 4.0E-06 144
rs121913237 0.611 0.560 1 114716126 missense variant C/A;G;T snv 8.0E-06 50
rs762846821 0.614 0.320 17 7675151 missense variant C/A;T snv 8.0E-06 57
rs121434569 0.581 0.520 7 55181378 missense variant C/T snv 2.8E-05 5.6E-05 70
rs1800470 0.515 0.840 19 41353016 missense variant G/A;C snv 0.55; 2.4E-04 107
rs2070600 0.561 0.760 6 32183666 missense variant C/T snv 5.3E-02 3.6E-02 82
rs11662595 0.882 0.120 18 24477006 missense variant A/G snv 8.6E-02 7.6E-02 7
rs16932912 0.882 0.120 9 36087879 missense variant G/A snv 9.2E-02 8.5E-02 5
rs1136410 0.559 0.760 1 226367601 missense variant A/G snv 0.21 0.15 70
rs1870377
KDR
0.695 0.520 4 55106807 missense variant T/A snv 0.22 0.20 25