Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2070744 | 0.608 | 0.680 | 7 | 150992991 | intron variant | C/T | snv | 0.70 | 54 | ||
rs2279744 | 0.605 | 0.640 | 12 | 68808800 | intron variant | T/G | snv | 0.31 | 48 | ||
rs3761548 | 0.620 | 0.680 | X | 49261784 | intron variant | G/A;T | snv | 42 | |||
rs4939827 | 0.708 | 0.160 | 18 | 48927093 | intron variant | T/A;C | snv | 25 | |||
rs966423 | 0.776 | 0.200 | 2 | 217445617 | intron variant | C/G;T | snv | 11 | |||
rs3212948 | 0.776 | 0.160 | 19 | 45421104 | intron variant | G/C | snv | 0.53 | 10 | ||
rs4648068 | 0.790 | 0.240 | 4 | 102597148 | intron variant | A/G | snv | 0.31 | 9 | ||
rs3021094 | 0.827 | 0.360 | 1 | 206771607 | intron variant | T/G | snv | 8.0E-02 | 8 | ||
rs4024 | 0.827 | 0.120 | 4 | 73435667 | intron variant | G/A | snv | 0.52 | 7 | ||
rs737241 | 0.827 | 0.120 | 4 | 73451012 | intron variant | G/A;C | snv | 7 | |||
rs738791 | 0.851 | 0.120 | 22 | 23775338 | intron variant | C/T | snv | 0.37 | 6 | ||
rs2289937 | 0.882 | 0.080 | 8 | 116861572 | intron variant | G/A;C | snv | 4 | |||
rs2835931 | 1.000 | 0.120 | 21 | 37749345 | intron variant | C/A;T | snv | 4 | |||
rs3917412 | 1.000 | 0.040 | 1 | 169731361 | intron variant | T/A;C;G | snv | 4 | |||
rs4579555 | 0.882 | 0.080 | 8 | 116867092 | intron variant | A/G | snv | 4 | |||
rs477145 | 1.000 | 0.120 | 21 | 31390097 | intron variant | C/A;T | snv | 4 | |||
rs9679162 | 0.882 | 0.120 | 2 | 31024648 | intron variant | G/T | snv | 0.48 | 4 | ||
rs4328905 | 4 | 83322396 | intron variant | A/G | snv | 0.18 | 0.18 | 1 | |||
rs6737848 | 2 | 46701027 | intron variant | C/G | snv | 0.14 | 1 | ||||
rs4769793 | 0.807 | 0.120 | 13 | 29985289 | intergenic variant | G/C | snv | 8 | |||
rs7240004 | 1.000 | 0.040 | 18 | 48868651 | intergenic variant | A/G | snv | 0.43 | 4 | ||
rs2660852 | 12 | 96051770 | intergenic variant | C/A | snv | 0.34 | 3 | ||||
rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 | ||
rs1114167628 | 0.925 | 0.080 | 10 | 87961033 | stop gained | -/ATATCTAG | delins | 5 | |||
rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 490 |