Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs174577 | 1.000 | 0.080 | 11 | 61837342 | intron variant | C/A | snv | 0.38 | 13 | ||
rs6801957 | 1.000 | 0.080 | 3 | 38725824 | intron variant | T/C | snv | 0.67 | 7 | ||
rs11894252 | 0.925 | 0.120 | 2 | 46306237 | intron variant | T/A;C;G | snv | 3 | |||
rs452036 | 14 | 23396676 | intron variant | G/A;C | snv | 0.33 | 3 | ||||
rs6790396 | 1.000 | 0.080 | 3 | 38730434 | intron variant | C/G | snv | 0.67 | 3 | ||
rs3922844 | 3 | 38582762 | intron variant | T/C | snv | 0.61 | 3 | ||||
rs7312625 | 1.000 | 0.080 | 12 | 114362169 | intron variant | G/A | snv | 0.71 | 3 | ||
rs11689011 | 1.000 | 0.120 | 2 | 46314037 | intron variant | T/A;C;G | snv | 2 | |||
rs2798334 | 1 | 111894722 | intron variant | T/C;G | snv | 2 | |||||
rs41312411 | 3 | 38579746 | intron variant | C/G | snv | 0.11 | 2 | ||||
rs1895582 | 12 | 114369230 | intron variant | G/A | snv | 0.70 | 2 | ||||
rs1467026 | 3 | 12789276 | upstream gene variant | G/A | snv | 0.67 | 1 | ||||
rs4276421 | 5 | 45801977 | intergenic variant | C/T | snv | 0.51 | 1 | ||||
rs2285703 | 4 | 113467664 | intron variant | A/G | snv | 0.21 | 1 | ||||
rs13242816 | 7 | 116549322 | intron variant | C/T | snv | 7.6E-02 | 1 | ||||
rs3801995 | 7 | 116550543 | intron variant | C/T | snv | 0.29 | 1 | ||||
rs562408 | 1 | 54276945 | intron variant | A/G | snv | 0.61 | 1 | ||||
rs148020424 | 12 | 114367252 | intron variant | -/AAAGAAAAGAGAAA;AGAAA | ins | 1 |