Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs565021665 | 1 | 159313100 | downstream gene variant | TTTTTTTTTTTTTT/-;TTTTT;TTTTTTT;TTTTTTTT;TTTTTTTTT;TTTTTTTTTT;TTTTTTTTTTT;TTTTTTTTTTTT;TTTTTTTTTTTTT;TTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTT;TTTTTTTTTTTTTTTTTTTTTTT | delins | 7.4E-02 | 1 | ||||
rs35163651 | 6 | 41086523 | intron variant | TTTT/-;TTT;TTTTT;TTTTTT | delins | 1 | |||||
rs34208856 | 6 | 135099930 | intron variant | TT/-;T;TTT;TTTTTTTTT | delins | 6 | |||||
rs34687215 | 1 | 224394506 | intron variant | TT/-;T;TTT;TTTTT;TTTTTT;TTTTTTT | delins | 0.19 | 1 | ||||
rs140740457 | 11 | 122629782 | regulatory region variant | TT/-;T;TTT;TTTTT | delins | 0.13 | 1 | ||||
rs397731840 | 8 | 129599504 | intron variant | TT/-;T;TTT;TTTT;TTTTT | delins | 5 | |||||
rs74267027 | 17 | 16268374 | intron variant | TT/- | delins | 0.40 | 3 | ||||
rs146318841 | 6 | 135328483 | intron variant | TGCCATAAACCATAGCCATAG/-;TGCCATAAACCATAGCCATAGTGCCATAAACCATAGCCATAG | delins | 4 | |||||
rs139707092 | 2 | 168850753 | intron variant | TCTCTGGAAT/-;TCTCTGGAATTCTCTGGAAT | delins | 5 | |||||
rs138171347 | 17 | 5279909 | upstream gene variant | TAAA/-;TAAATAAA | delins | 1 | |||||
rs78378222 | 0.662 | 0.360 | 17 | 7668434 | 3 prime UTR variant | T/G | snv | 8.3E-03 | 37 | ||
rs9260620 | 6 | 29955314 | upstream gene variant | T/G | snv | 0.24 | 7 | ||||
rs2785663 | 1.000 | 0.040 | 1 | 157650968 | intergenic variant | T/G | snv | 0.64 | 2 | ||
rs3557 | 1 | 161219103 | 3 prime UTR variant | T/G | snv | 6.5E-02 | 2 | ||||
rs6846071 | 4 | 101481058 | intron variant | T/G | snv | 0.15 | 2 | ||||
rs10840291 | 11 | 9708594 | intron variant | T/G | snv | 0.34 | 1 | ||||
rs11602323 | 11 | 122648573 | regulatory region variant | T/G | snv | 0.14 | 1 | ||||
rs117342529 | 8 | 21853230 | intergenic variant | T/G | snv | 2.6E-02 | 1 | ||||
rs12074934 | 1 | 159338281 | intergenic variant | T/G | snv | 0.19 | 1 | ||||
rs12144133 | 1 | 10144128 | intron variant | T/G | snv | 0.37 | 1 | ||||
rs12740969 | 1 | 154514584 | intron variant | T/G | snv | 0.50 | 1 | ||||
rs17038861 | 2 | 37006122 | intron variant | T/G | snv | 0.18 | 1 | ||||
rs1997814 | 20 | 10666023 | intron variant | T/G | snv | 0.73 | 1 | ||||
rs2227336 | 17 | 40018602 | upstream gene variant | T/G | snv | 0.36 | 1 | ||||
rs2247584 | 1 | 159289890 | intron variant | T/G | snv | 0.34 | 1 |