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 | 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 |