Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1983127 | 10 | 69230145 | intron variant | G/T | snv | 0.38 | 2 | ||||
rs2268575 | 7 | 44149675 | intron variant | T/C | snv | 0.18 | 2 | ||||
rs2280231 | 11 | 47578886 | 5 prime UTR variant | C/T | snv | 0.24 | 0.20 | 2 | |||
rs2300615 | 6 | 39071727 | intron variant | T/G | snv | 0.17 | 2 | ||||
rs2302593 | 19 | 45693376 | intron variant | C/A;G | snv | 1.0E-04; 0.48 | 2 | ||||
rs2390732 | 2 | 168749457 | intron variant | G/A | snv | 0.65 | 2 | ||||
rs2605627 | 11 | 93526349 | intron variant | A/G | snv | 0.79 | 2 | ||||
rs2971671 | 7 | 44171738 | intron variant | T/C | snv | 0.22 | 2 | ||||
rs2979422 | 7 | 44122756 | intron variant | T/C | snv | 0.20 | 2 | ||||
rs3138708 | 3 | 171009914 | intron variant | T/G | snv | 3.1E-02 | 2 | ||||
rs340878 | 1 | 213983706 | intron variant | G/C | snv | 0.63 | 2 | ||||
rs35859536 | 8 | 117179236 | downstream gene variant | C/T | snv | 0.25 | 2 | ||||
rs3778321 | 6 | 7250037 | 3 prime UTR variant | G/A | snv | 0.11 | 2 | ||||
rs3783347 | 14 | 100372924 | intron variant | G/T | snv | 0.16 | 2 | ||||
rs3816725 | 11 | 47284118 | intron variant | T/C;G | snv | 2 | |||||
rs3829109 | 9 | 136362314 | intron variant | G/A | snv | 0.25 | 2 | ||||
rs4237150 | 9 | 4290085 | intron variant | G/A;C;T | snv | 2 | |||||
rs4775471 | 15 | 62132450 | intergenic variant | C/T | snv | 0.18 | 2 | ||||
rs4869272 | 5 | 96203744 | intron variant | C/T | snv | 0.72 | 2 | ||||
rs5394 | 3 | 171027104 | intron variant | G/A | snv | 0.15 | 2 | ||||
rs6072275 | 20 | 41115265 | intron variant | G/A | snv | 0.13 | 2 | ||||
rs6113722 | 20 | 22576461 | intron variant | G/A;T | snv | 2 | |||||
rs6943153 | 7 | 50723882 | intron variant | T/C | snv | 0.56 | 2 | ||||
rs6975024 | 7 | 44192287 | intron variant | T/C | snv | 0.14 | 2 | ||||
rs7101470 | 11 | 47032897 | intron variant | A/G | snv | 7.4E-02 | 2 |