Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs997050266 | 0.851 | 0.120 | 19 | 45423352 | missense variant | T/A;C | snv | 1.4E-05 | 4 | ||
rs9939609 | 0.559 | 0.720 | 16 | 53786615 | intron variant | T/A | snv | 0.41 | 98 | ||
rs9904341 | 0.695 | 0.280 | 17 | 78214286 | 5 prime UTR variant | G/A;C;T | snv | 0.38; 4.8E-06 | 20 | ||
rs9838411 | 0.925 | 0.080 | 3 | 179169899 | intron variant | G/A | snv | 0.25 | 2 | ||
rs9668337 | 1.000 | 0.080 | 12 | 26273405 | non coding transcript exon variant | G/A | snv | 0.55 | 1 | ||
rs9639594 | 1.000 | 0.080 | 7 | 29139570 | intron variant | G/A | snv | 0.20 | 1 | ||
rs9600103 | 1.000 | 0.080 | 13 | 73237742 | intergenic variant | A/T | snv | 0.33 | 1 | ||
rs944050 | 0.827 | 0.280 | 14 | 64233327 | splice region variant | T/C | snv | 9.5E-02 | 7.9E-02 | 5 | |
rs937213 | 1.000 | 0.080 | 15 | 40029923 | intron variant | T/C | snv | 0.31 | 3 | ||
rs9340799 | 0.583 | 0.680 | 6 | 151842246 | intron variant | A/G | snv | 0.32 | 62 | ||
rs9282861 | 0.658 | 0.440 | 16 | 28606193 | missense variant | C/T | snv | 31 | |||
rs9261204 | 0.790 | 0.200 | 6 | 30037466 | intron variant | A/G | snv | 0.17 | 9 | ||
rs911162 | 1.000 | 0.080 | 20 | 56391393 | intron variant | A/C;G | snv | 1 | |||
rs892119 | 0.925 | 0.080 | 19 | 40254165 | intron variant | C/T | snv | 0.19 | 2 | ||
rs889312 | 0.732 | 0.360 | 5 | 56736057 | regulatory region variant | C/A | snv | 0.69 | 14 | ||
rs887829 | 0.763 | 0.280 | 2 | 233759924 | intron variant | C/T | snv | 0.36 | 18 | ||
rs886039484 | 0.641 | 0.440 | 17 | 7674888 | missense variant | T/C;G | snv | 32 | |||
rs882380 | 1.000 | 0.080 | 17 | 48216874 | intron variant | C/A | snv | 0.52 | 1 | ||
rs878854066 | 0.439 | 0.800 | 17 | 7676153 | missense variant | GG/AC | mnv | 213 | |||
rs876660943 | 0.882 | 0.240 | 2 | 47806359 | splice donor variant | G/T | snv | 7.0E-06 | 5 | ||
rs876658932 | 0.807 | 0.400 | 16 | 68801726 | stop gained | C/G;T | snv | 7 | |||
rs872267 | 1.000 | 0.080 | 3 | 128169224 | intron variant | G/A | snv | 0.43 | 1 | ||
rs864622149 | 0.851 | 0.160 | 22 | 28710005 | splice donor variant | C/A;G;T | snv | 5 | |||
rs864622121 | 1.000 | 0.080 | 2 | 47475228 | frameshift variant | GT/- | del | 2 | |||
rs861539 | 0.519 | 0.680 | 14 | 103699416 | missense variant | G/A | snv | 0.29 | 0.30 | 104 |