Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800795 | 0.494 | 0.840 | 7 | 22727026 | intron variant | C/G | snv | 0.71 | 140 | ||
rs12203592 | 0.649 | 0.320 | 6 | 396321 | intron variant | C/T | snv | 0.10 | 38 | ||
rs16901979 | 0.724 | 0.480 | 8 | 127112671 | intron variant | C/A | snv | 0.16 | 17 | ||
rs2242652 | 0.724 | 0.400 | 5 | 1279913 | intron variant | G/A | snv | 0.18 | 16 | ||
rs2235544 | 0.742 | 0.240 | 1 | 53909897 | intron variant | C/A;T | snv | 0.53; 4.0E-06 | 14 | ||
rs12621278 | 0.790 | 0.280 | 2 | 172446825 | intron variant | A/G | snv | 4.9E-02 | 7 | ||
rs6465657 | 0.807 | 0.280 | 7 | 98187015 | intron variant | C/T | snv | 0.41 | 0.37 | 7 | |
rs210143 | 0.827 | 0.160 | 6 | 33579153 | intron variant | T/C | snv | 0.74 | 6 | ||
rs4533622 | 0.807 | 0.240 | 3 | 41200847 | intron variant | C/A;T | snv | 6 | |||
rs4693608 | 0.827 | 0.200 | 4 | 83320204 | intron variant | G/A;C | snv | 6 | |||
rs2456449 | 0.827 | 0.280 | 8 | 127180736 | intron variant | A/G | snv | 0.30 | 5 | ||
rs4459895 | 0.827 | 0.160 | 3 | 188236626 | intron variant | A/C | snv | 0.88 | 5 | ||
rs7336610 | 0.827 | 0.240 | 13 | 91352883 | intron variant | C/T | snv | 0.47 | 5 | ||
rs9372120 | 0.851 | 0.280 | 6 | 106219660 | intron variant | T/G | snv | 0.16 | 5 | ||
rs11715604 | 0.851 | 0.160 | 3 | 136870707 | intron variant | A/G;T | snv | 4 | |||
rs12147254 | 0.851 | 0.240 | 14 | 102799329 | intron variant | G/A | snv | 0.23 | 4 | ||
rs131821 | 0.851 | 0.160 | 22 | 50511648 | intron variant | T/-;TT;TTT;TTTT | delins | 4 | |||
rs149207840 | 0.851 | 0.160 | 2 | 230279864 | intron variant | CTGCCTC/-;CTGCCTCCTGCCTC | delins | 0.15 | 4 | ||
rs181181503 | 0.851 | 0.160 | 12 | 74276187 | intron variant | T/C | snv | 1.5E-03 | 4 | ||
rs1934951 | 0.925 | 0.160 | 10 | 95038791 | intron variant | C/T | snv | 0.24 | 4 | ||
rs2546191 | 0.851 | 0.160 | 5 | 95896837 | intron variant | G/A | snv | 0.38 | 4 | ||
rs2720680 | 0.851 | 0.160 | 8 | 128102971 | intron variant | A/G | snv | 0.33 | 4 | ||
rs35603048 | 0.851 | 0.160 | 15 | 40099764 | intron variant | C/A;G;T | snv | 4 | |||
rs4240803 | 0.851 | 0.240 | 16 | 87855597 | intron variant | G/A;C;T | snv | 4 | |||
rs4273077 | 0.925 | 0.160 | 17 | 16945825 | intron variant | A/G | snv | 0.13 | 4 |