Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs12917707 | 0.827 | 0.200 | 16 | 20356368 | upstream gene variant | G/T | snv | 0.14 | 11 | ||
rs12979860 | 0.547 | 0.520 | 19 | 39248147 | intron variant | C/T | snv | 0.39 | 84 | ||
rs1317776692 | 14 | 104701619 | missense variant | C/G;T | snv | 4.4E-06 | 1 | ||||
rs13293564 | 9 | 35166766 | intron variant | G/A;T | snv | 1 | |||||
rs1332629192 | 0.851 | 0.200 | 4 | 73404374 | missense variant | C/T | snv | 7 | |||
rs13333226 | 0.827 | 0.200 | 16 | 20354332 | intron variant | A/G | snv | 0.23 | 10 | ||
rs1337503417 | 0.790 | 0.160 | 17 | 41612325 | missense variant | G/T | snv | 4.0E-06 | 12 | ||
rs136161 | 0.925 | 0.160 | 22 | 36261386 | intron variant | G/C | snv | 0.51 | 3 | ||
rs140511594 | 0.742 | 0.360 | 2 | 165941111 | missense variant | G/A | snv | 1.3E-04 | 1.1E-04 | 13 | |
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs1427118369 | 2 | 227283830 | missense variant | G/A | snv | 4.0E-06 | 1.4E-05 | 1 | |||
rs146956976 | 1.000 | 0.080 | 9 | 121302985 | missense variant | C/T | snv | 3.1E-04 | 4.0E-04 | 2 | |
rs1524107 | 0.827 | 0.320 | 7 | 22728600 | non coding transcript exon variant | C/T | snv | 9.4E-02 | 6 | ||
rs16139 | 0.658 | 0.560 | 7 | 24285260 | missense variant | T/A;C | snv | 4.0E-06; 3.0E-02 | 36 | ||
rs1617640 | 0.742 | 0.520 | 7 | 100719675 | upstream gene variant | C/A;G;T | snv | 15 | |||
rs17880135 | 21 | 31669690 | upstream gene variant | T/G | snv | 3.9E-02 | 1 | ||||
rs17881180 | 21 | 31659974 | non coding transcript exon variant | C/T | snv | 3.8E-02 | 1 | ||||
rs17883901 | 0.851 | 0.240 | 6 | 53545239 | intron variant | G/A;T | snv | 6.2E-02 | 6 | ||
rs1799752 | 0.677 | 0.480 | 17 | 63488529 | intron variant | -/TTTTTTTTTTTGAGACGGAGTCTCGCTCTGTCGCCCATACAGTCACTTTT | delins | 25 | |||
rs1799864 | 0.572 | 0.680 | 3 | 46357717 | missense variant | G/A | snv | 0.13 | 0.12 | 68 | |
rs1799883 | 0.658 | 0.440 | 4 | 119320747 | missense variant | T/A;C;G | snv | 0.73 | 36 | ||
rs1799945 | 0.452 | 0.760 | 6 | 26090951 | missense variant | C/G;T | snv | 0.11 | 0.10 | 226 | |
rs1799983 | 0.430 | 0.880 | 7 | 150999023 | missense variant | T/A;G | snv | 0.75 | 246 | ||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 | |
rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 |