Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs867114783 | 17 | 7675109 | missense variant | T/C | snv | 5 | |||||
rs80359030 | 0.851 | 13 | 32363189 | stop gained | G/A;T | snv | 4.0E-06 | 5 | |||
rs886040738 | 0.851 | 13 | 32363188 | frameshift variant | G/- | delins | 5 | ||||
rs200484060 | 1.000 | 18 | 31536370 | missense variant | T/G | snv | 5.6E-05 | 1.4E-05 | 4 | ||
rs1269252748 | 9 | 2641436 | missense variant | C/T | snv | 4 | |||||
rs760361706 | 22 | 46235326 | missense variant | G/C | snv | 4.0E-06 | 4 | ||||
rs9983925 | 21 | 45216929 | intron variant | C/T | snv | 0.46 | 4 | ||||
rs876660427 | 5 | 112838608 | missense variant | C/T | snv | 4 | |||||
rs140516819 | 7 | 55172999 | missense variant | A/C;G | snv | 4.0E-05 | 2.4E-04 | 4 | |||
rs35918369 | 7 | 55205613 | missense variant | C/T | snv | 3.1E-04 | 3.3E-04 | 4 | |||
rs1018379423 | 1 | 22907986 | missense variant | G/T | snv | 4.0E-06 | 2.1E-05 | 4 | |||
rs767136747 | 9 | 133717404 | missense variant | T/C | snv | 4.0E-06 | 4 | ||||
rs1441008398 | 5 | 112839334 | missense variant | C/T | snv | 4.0E-06 | 4 | ||||
rs750605522 | 16 | 58722168 | missense variant | T/A | snv | 4.0E-06 | 7.0E-06 | 4 | |||
rs3136558 | 1.000 | 2 | 112833698 | intron variant | A/G | snv | 0.21 | 4 | |||
rs7668666 | 1.000 | 4 | 186080138 | intron variant | C/A;T | snv | 4 | ||||
rs863224683 | 17 | 7675224 | missense variant | G/A;C | snv | 4 | |||||
rs1057518011 | 1 | 1535766 | missense variant | C/T | snv | 4 | |||||
rs121434591 | 1.000 | 5 | 139307669 | missense variant | C/G | snv | 4 | ||||
rs211105 | 1.000 | 11 | 18033757 | intron variant | T/G | snv | 0.19 | 4 | |||
rs2640909 | 1 | 7830057 | missense variant | T/C | snv | 0.14 | 0.23 | 4 | |||
rs201920319 | 0.925 | 5 | 157731604 | missense variant | T/C | snv | 2.1E-04 | 1.2E-04 | 4 | ||
rs587777570 | 1.000 | 2 | 148947018 | missense variant | G/A | snv | 3 | ||||
rs1052108705 | 6 | 31165217 | missense variant | C/T | snv | 4.1E-06 | 2.1E-05 | 3 | |||
rs768746587 | 6 | 31165136 | missense variant | C/T | snv | 8.4E-06 | 3 |