Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs200484060 | 1.000 | 18 | 31536370 | missense variant | T/G | snv | 5.6E-05 | 1.4E-05 | 4 | ||
rs1057518905 | 1 | 155140104 | missense variant | A/T | snv | 3 | |||||
rs143137713 | 0.925 | 3 | 148996462 | missense variant | G/C | snv | 1.0E-03 | 1.1E-03 | 3 | ||
rs4746172 | 10 | 74096084 | intron variant | C/T | snv | 0.73 | 3 | ||||
rs587777425 | 1.000 | 1 | 160237145 | missense variant | G/A;T | snv | 3 | ||||
rs1334828551 | 1 | 20500800 | missense variant | A/G | snv | 4.0E-06 | 1.4E-05 | 2 | |||
rs1343372308 | 14 | 23413792 | missense variant | C/G | snv | 7.0E-06 | 2 | ||||
rs1393142163 | 10 | 67521867 | missense variant | T/C | snv | 2 | |||||
rs202238194 | 1.000 | 1 | 74492217 | missense variant | G/A;C | snv | 1.6E-05 | 2 | |||
rs267607577 | 1 | 156136352 | frameshift variant | GCACGCAC/-;GCACGCACGCAC | delins | 2 | |||||
rs368200299 | 2 | 178620285 | stop gained | G/A;T | snv | 4.9E-06 | 2 | ||||
rs371855540 | 14 | 23415095 | missense variant | C/T | snv | 2.0E-05 | 3.5E-05 | 2 | |||
rs45516091 | 14 | 23431608 | missense variant | G/A | snv | 1.2E-05 | 7.0E-06 | 2 | |||
rs727504466 | 2 | 178591326 | frameshift variant | T/- | del | 2 | |||||
rs727504799 | 2 | 178609683 | splice donor variant | C/G | snv | 2 | |||||
rs746365549 | 2 | 178782573 | missense variant | C/A;T | snv | 8.0E-06 | 2 | ||||
rs760185784 | 18 | 31089533 | missense variant | T/C | snv | 4.0E-06 | 2 | ||||
rs869312054 | 2 | 178593566 | splice donor variant | A/G | snv | 1.4E-05 | 2 | ||||
rs876657670 | 2 | 178560622 | stop gained | C/A;T | snv | 2 | |||||
rs1024095026 | 12 | 21887879 | stop gained | G/A | snv | 1.2E-05 | 1 | ||||
rs1057519457 | 19 | 35033599 | missense variant | A/T | snv | 1 | |||||
rs1060500235 | 1 | 201365657 | missense variant | T/C;G | snv | 1 | |||||
rs12582717 | 12 | 21143872 | intron variant | C/G | snv | 4.1E-02 | 1 | ||||
rs1286964261 | 11 | 66003356 | missense variant | G/A | snv | 7.0E-06 | 1 | ||||
rs141735183 | 14 | 23420222 | stop gained | C/A | snv | 8.2E-06 | 7.0E-06 | 1 |