Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs7074891 0.925 0.120 10 17146475 3 prime UTR variant C/T snv 0.95 2
rs7015626 1.000 0.120 8 124864572 intron variant G/A snv 0.39 1
rs698 0.724 0.240 4 99339632 missense variant T/A;C snv 0.35 20
rs671 0.529 0.840 12 111803962 missense variant G/A snv 1.9E-02 5.8E-03 116
rs6475609 0.925 0.120 9 22106272 intron variant A/C;G;T snv 2
rs6464375 0.925 0.120 7 153928758 intron variant C/T snv 6.7E-02 2
rs63751412 0.882 0.200 2 47429869 stop gained C/A;G;T snv 8.0E-06; 4.0E-06 4
rs6214 0.672 0.400 12 102399791 3 prime UTR variant C/T snv 0.45 26
rs62068300 0.925 0.120 17 80600927 intron variant G/A;T snv 5.7E-05 2
rs6127119 0.925 0.120 20 54162543 intron variant C/T snv 0.24 2
rs6001516 0.925 0.120 22 39248198 intron variant C/T snv 6.1E-02 2
rs587779067 0.882 0.200 2 47416399 missense variant C/G;T snv 5
rs587778992 0.882 0.200 3 37050606 stop gained C/T snv 4
rs587778883 0.807 0.200 3 37025648 frameshift variant A/- del 7
rs587776416 0.882 0.240 16 23629986 frameshift variant AT/- del 6.4E-05 2.1E-05 5
rs5768709 0.925 0.120 22 48533757 intron variant A/G snv 0.36 2
rs5757573 0.925 0.120 22 39237617 intron variant C/T snv 0.57 2
rs56053615 0.851 0.120 3 9751845 missense variant G/A;T snv 3.4E-04; 4.0E-06 4
rs5361 0.623 0.720 1 169731919 missense variant T/G snv 8.3E-02; 8.0E-06 7.8E-02 47
rs5352 0.827 0.200 13 77901095 missense variant C/T snv 1.0E-02 1.1E-02 5
rs5219 0.701 0.360 11 17388025 stop gained T/A;C snv 0.64 25
rs505922
ABO
0.689 0.520 9 133273813 intron variant C/T snv 34
rs4994 0.578 0.640 8 37966280 missense variant A/G snv 0.11 9.2E-02 65
rs4988487 0.925 0.120 16 1079193 missense variant C/A;T snv 4.0E-06; 5.3E-02 2
rs4988483 0.752 0.240 16 1079010 missense variant C/A snv 3.7E-02 3.7E-02 11