Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 23 | |||||
rs11066280 | 0.742 | 0.280 | 12 | 112379979 | intron variant | T/A | snv | 7.0E-03 | 13 | ||
rs2896019 | 0.790 | 0.160 | 22 | 43937814 | intron variant | T/G | snv | 0.20 | 8 | ||
rs333947 | 1 | 109928142 | intron variant | G/A | snv | 0.13 | 7 | ||||
rs3747207 | 22 | 43928975 | intron variant | G/A | snv | 0.22 | 7 | ||||
rs11878604 | 19 | 40827379 | intron variant | T/C | snv | 0.14 | 5 | ||||
rs4835265 | 4 | 145900258 | intron variant | C/A | snv | 0.15 | 5 | ||||
rs4823173 | 0.827 | 0.200 | 22 | 43932850 | intron variant | G/A | snv | 0.24 | 0.18 | 4 | |
rs12231737 | 0.925 | 0.120 | 12 | 112136812 | intron variant | C/T | snv | 5.9E-03 | 3 | ||
rs13077101 | 3 | 120706484 | intron variant | T/C | snv | 3 | |||||
rs139761834 | 7 | 80545045 | intron variant | T/C | snv | 2.8E-04 | 3 | ||||
rs1818782 | 5 | 39424526 | intron variant | A/C | snv | 0.56 | 3 | ||||
rs2078087 | 1 | 183389270 | intron variant | C/T | snv | 0.16 | 3 | ||||
rs2241339 | 2 | 169013785 | intron variant | C/A;T | snv | 3 | |||||
rs34010237 | 19 | 49509317 | intron variant | G/A | snv | 0.13 | 3 | ||||
rs4949718 | 1 | 76433779 | intron variant | T/A;C | snv | 3 | |||||
rs74913549 | 11 | 94180526 | intron variant | T/A;C | snv | 3 | |||||
rs892295 | 3 | 355870 | intron variant | A/G | snv | 0.87 | 3 | ||||
rs9389268 | 1.000 | 0.080 | 6 | 135098493 | intron variant | A/G | snv | 0.24 | 3 | ||
rs10272006 | 0.925 | 0.080 | 7 | 21480514 | intron variant | G/A | snv | 0.75 | 2 | ||
rs11820744 | 1.000 | 0.040 | 11 | 3147308 | intron variant | C/T | snv | 0.23 | 2 | ||
rs139271658 | 1.000 | 0.040 | 9 | 9797383 | intron variant | A/G | snv | 1.9E-02 | 2 | ||
rs4598207 | 7 | 50218883 | intron variant | A/T | snv | 0.34 | 2 | ||||
rs10165093 | 2 | 232639279 | intron variant | G/A | snv | 0.41 | 1 | ||||
rs10198552 | 2 | 134842306 | intron variant | T/C | snv | 6.2E-02 | 1 |