Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1050153 | 0.925 | 0.120 | 3 | 196049444 | 3 prime UTR variant | G/A | snv | 2 | |||
rs10519068 | 0.925 | 0.120 | 15 | 60776505 | intron variant | G/A | snv | 0.22 | 2 | ||
rs1058808 | 0.658 | 0.360 | 17 | 39727784 | missense variant | C/G | snv | 0.61 | 0.52 | 27 | |
rs1059513 | 0.776 | 0.240 | 12 | 57095926 | 3 prime UTR variant | T/C | snv | 8.0E-02 | 11 | ||
rs10791824 | 0.882 | 0.160 | 11 | 65791795 | intron variant | A/G;T | snv | 3 | |||
rs112401631 | 0.882 | 0.120 | 17 | 40608272 | TF binding site variant | T/A | snv | 1.1E-02 | 8 | ||
rs115288876 | 0.925 | 0.120 | 1 | 152027641 | intron variant | G/A | snv | 2.5E-02 | 3 | ||
rs11558538 | 0.695 | 0.400 | 2 | 138002079 | missense variant | C/T | snv | 1.0E-01 | 8.4E-02 | 19 | |
rs11584340 | 0.827 | 0.200 | 1 | 152313454 | missense variant | G/A | snv | 0.27 | 0.19 | 5 | |
rs117137535 | 0.882 | 0.120 | 9 | 137605991 | intron variant | G/A | snv | 2.7E-02 | 3 | ||
rs1214598 | 0.925 | 0.120 | 1 | 167457187 | non coding transcript exon variant | G/A;C;T | snv | 3 | |||
rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
rs12186803 | 0.925 | 0.120 | 5 | 132704377 | intron variant | G/A;C | snv | 2 | |||
rs12365699 | 0.882 | 0.120 | 11 | 118872577 | regulatory region variant | G/A | snv | 0.12 | 5 | ||
rs1295685 | 0.790 | 0.160 | 5 | 132660753 | 3 prime UTR variant | A/G | snv | 0.81 | 7 | ||
rs13277355 | 0.882 | 0.120 | 8 | 127765473 | intergenic variant | A/G | snv | 0.71 | 3 | ||
rs13360927 | 0.882 | 0.160 | 5 | 110700055 | intron variant | A/G | snv | 9.3E-02 | 3 | ||
rs13361382 | 0.882 | 0.160 | 5 | 110713253 | intron variant | G/A | snv | 9.3E-02 | 3 | ||
rs1342326 | 0.790 | 0.360 | 9 | 6190076 | intergenic variant | A/C | snv | 0.21 | 9 | ||
rs138726443 | 0.790 | 0.200 | 1 | 152307547 | stop gained | G/A;C;T | snv | 2.8E-03; 4.0E-06; 1.6E-05 | 7 | ||
rs1444782 | 0.851 | 0.240 | 10 | 9016708 | intergenic variant | G/A | snv | 0.35 | 5 | ||
rs150597413 | 0.827 | 0.160 | 1 | 152305146 | stop gained | G/A;C;T | snv | 3.6E-05; 4.0E-06; 1.5E-03 | 5 | ||
rs1544410 | 0.542 | 0.760 | 12 | 47846052 | intron variant | C/A;G;T | snv | 78 | |||
rs1555549674 | 0.882 | 0.240 | 17 | 42223402 | missense variant | T/G | snv | 6 | |||
rs167769 | 0.827 | 0.280 | 12 | 57109992 | 5 prime UTR variant | C/T | snv | 0.31 | 5 |