Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7742369 | 6 | 34197944 | TF binding site variant | A/G | snv | 0.30 | 1 | ||||
rs7968682 | 12 | 65978100 | intergenic variant | G/T | snv | 0.56 | 1 | ||||
rs930811 | 9 | 2696555 | intergenic variant | G/A | snv | 0.47 | 1 | ||||
rs9883204 | 3 | 123377973 | intron variant | T/A;C | snv | 1 | |||||
rs1801253 | 0.683 | 0.440 | 10 | 114045297 | missense variant | G/C | snv | 0.74 | 0.69 | 1 | |
rs798489 | 7 | 2762169 | splice donor variant | C/T | snv | 0.20 | 1 | ||||
rs7780752 | 7 | 93612328 | intron variant | T/C | snv | 0.27 | 1 | ||||
rs1351394 | 12 | 65958046 | 3 prime UTR variant | T/C;G | snv | 1 | |||||
rs8756 | 0.882 | 0.200 | 12 | 65965972 | 3 prime UTR variant | C/A | snv | 0.56 | 1 | ||
rs2928148 | 15 | 41109352 | intron variant | G/A | snv | 0.44 | 1 | ||||
rs11867479 | 17 | 70094066 | intron variant | C/A;T | snv | 1 | |||||
rs1415701 | 6 | 130024690 | intron variant | G/A | snv | 0.31 | 1 | ||||
rs925098 | 4 | 17918188 | intron variant | G/A | snv | 0.70 | 1 | ||||
rs900400 | 0.925 | 0.080 | 3 | 157080986 | upstream gene variant | T/C | snv | 0.36 | 1 | ||
rs3107997 | 18 | 30340278 | intron variant | C/T | snv | 0.21 | 1 | ||||
rs809871 | 6 | 26256298 | downstream gene variant | C/G;T | snv | 1 | |||||
rs7849941 | 9 | 85130318 | intergenic variant | A/T | snv | 0.27 | 1 | ||||
rs2282978 | 7 | 92635096 | intron variant | T/C | snv | 0.38 | 1 | ||||
rs12461110 | 19 | 55809297 | missense variant | G/A | snv | 0.32 | 0.26 | 1 | |||
rs3918226 | 0.925 | 0.080 | 7 | 150993088 | intron variant | C/T | snv | 5.7E-02 | 1 | ||
rs3740360 | 0.827 | 0.240 | 10 | 94265734 | intron variant | A/C | snv | 9.7E-02 | 8.4E-02 | 1 | |
rs753381 | 20 | 41168825 | missense variant | T/C | snv | 0.61 | 0.67 | 1 | |||
rs2292626 | 0.925 | 0.120 | 10 | 122427198 | intron variant | C/T | snv | 0.46 | 1 | ||
rs670523 | 1.000 | 0.040 | 1 | 155908941 | intron variant | A/G | snv | 0.48 | 1 | ||
rs339969 | 15 | 60591082 | intron variant | C/A | snv | 0.68 | 1 |