Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7679673 | 0.677 | 0.440 | 4 | 105140377 | intron variant | C/A | snv | 0.50 | 23 | ||
rs7705526 | 0.776 | 0.240 | 5 | 1285859 | intron variant | C/A;T | snv | 15 | |||
rs13331259 | 16 | 249924 | intron variant | A/G | snv | 3.0E-02 | 14 | ||||
rs112505971 | 10 | 27068541 | intron variant | A/C;G | snv | 13 | |||||
rs3123543 | 1 | 212617344 | intron variant | T/A;C | snv | 13 | |||||
rs4837892 | 9 | 121826025 | intron variant | G/T | snv | 0.36 | 13 | ||||
rs7296503 | 12 | 41306962 | intron variant | C/T | snv | 0.57 | 13 | ||||
rs76792961 | 16 | 243594 | intron variant | C/T | snv | 7.3E-03 | 13 | ||||
rs9917425 | 20 | 16755400 | intron variant | G/T | snv | 0.16 | 13 | ||||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs445 | 7 | 92779056 | intron variant | C/T | snv | 0.14 | 9 | ||||
rs2954031 | 8 | 125479491 | intron variant | G/T | snv | 0.42 | 8 | ||||
rs12239046 | 1 | 247438293 | intron variant | T/C | snv | 0.58 | 7 | ||||
rs12266014 | 10 | 24922362 | intron variant | C/T | snv | 0.26 | 7 | ||||
rs2038700 | 14 | 24992783 | intron variant | T/C | snv | 0.53 | 7 | ||||
rs2524079 | 6 | 31274397 | intron variant | G/A | snv | 0.44 | 6 | ||||
rs2979489 | 8 | 30423317 | intron variant | G/A;C | snv | 6 | |||||
rs34208856 | 6 | 135099930 | intron variant | TT/-;T;TTT;TTTTTTTTT | delins | 6 | |||||
rs10075801 | 5 | 132341949 | intron variant | A/G | snv | 0.31 | 5 | ||||
rs10138752 | 14 | 68713254 | intron variant | C/T | snv | 8.8E-02 | 5 | ||||
rs10173538 | 2 | 159712765 | intron variant | C/G;T | snv | 5 | |||||
rs113542380 | 2 | 43237679 | intron variant | G/A | snv | 4.7E-02 | 5 | ||||
rs1144700 | 6 | 16744456 | intron variant | C/G;T | snv | 5 | |||||
rs11654074 | 17 | 59748211 | intron variant | A/C | snv | 0.40 | 5 | ||||
rs12550612 | 8 | 23109256 | intron variant | G/A | snv | 0.83 | 5 |