Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1173771 | 5 | 32814922 | regulatory region variant | A/G | snv | 0.65 | 9 | ||||
rs459193 | 0.925 | 0.120 | 5 | 56510924 | downstream gene variant | A/G | snv | 0.69 | 9 | ||
rs445 | 7 | 92779056 | intron variant | C/T | snv | 0.14 | 9 | ||||
rs45446698 | 0.807 | 0.120 | 7 | 99735325 | upstream gene variant | T/G | snv | 2.7E-02 | 9 | ||
rs6457374 | 0.851 | 0.200 | 6 | 31304484 | intron variant | C/T | snv | 0.81 | 9 | ||
rs11205303 | 0.882 | 0.120 | 1 | 149934520 | missense variant | T/C | snv | 0.33 | 0.29 | 9 | |
rs12967135 | 18 | 60181790 | intergenic variant | G/A | snv | 0.24 | 8 | ||||
rs2145272 | 20 | 6645571 | intergenic variant | G/A;T | snv | 8 | |||||
rs34811474 | 1.000 | 0.040 | 4 | 25407216 | missense variant | G/A;T | snv | 0.15; 4.1E-06 | 8 | ||
rs1966265 | 0.827 | 0.160 | 5 | 177089630 | missense variant | G/A;T | snv | 0.25 | 8 | ||
rs2011077 | 0.807 | 0.080 | 5 | 177094455 | intron variant | C/T | snv | 0.19 | 8 | ||
rs1182188 | 0.827 | 0.120 | 7 | 2830351 | intron variant | T/C | snv | 0.26 | 8 | ||
rs110419 | 0.827 | 0.200 | 11 | 8231306 | intron variant | A/G | snv | 0.42 | 8 | ||
rs6234 | 0.851 | 0.160 | 5 | 96393270 | missense variant | G/C | snv | 0.27 | 0.24 | 8 | |
rs3823418 | 0.925 | 0.120 | 6 | 31133165 | intron variant | G/A | snv | 0.23 | 8 | ||
rs35874463 | 0.827 | 0.120 | 15 | 67165360 | missense variant | A/G | snv | 4.0E-02 | 3.4E-02 | 8 | |
rs2066808 | 0.807 | 0.280 | 12 | 56344189 | intron variant | A/G | snv | 0.21 | 8 | ||
rs16948048 | 0.925 | 0.040 | 17 | 49363104 | intron variant | A/G | snv | 0.37 | 8 | ||
rs13437082 | 1.000 | 6 | 31386783 | upstream gene variant | C/T | snv | 0.32 | 7 | |||
rs33912345 | 0.807 | 0.200 | 14 | 60509819 | missense variant | C/A;G | snv | 0.53 | 7 | ||
rs7203984 | 16 | 56965346 | intron variant | A/C | snv | 0.31 | 7 | ||||
rs34517439 | 0.882 | 0.120 | 1 | 77984833 | intron variant | C/A | snv | 7.3E-02 | 7 | ||
rs6024836 | 0.851 | 0.160 | 20 | 56369012 | downstream gene variant | G/A | snv | 0.42 | 7 | ||
rs13108218 | 4 | 3442204 | intron variant | A/G;T | snv | 7 | |||||
rs7689420 | 0.851 | 0.080 | 4 | 144647200 | non coding transcript exon variant | T/C | snv | 0.79 | 7 |