| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs281875329 | 0.925 | 0.120 | 17 | 81511224 | missense variant | G/A;T | snv | 4.0E-06 | 3 | ||
| rs1555666392 | 1.000 | 17 | 81510814 | missense variant | C/T | snv | 2 | ||||
| rs281875330 | 1.000 | 0.120 | 17 | 81511626 | missense variant | T/C | snv | 2 | |||
| rs104894545 | 1.000 | 0.120 | 17 | 81510824 | missense variant | G/C | snv | 1 | |||
| rs104894547 | 1.000 | 0.120 | 17 | 81510709 | missense variant | A/G | snv | 1 | |||
| rs1140892 | 17 | 81510330 | splice acceptor variant | C/T | snv | 1.8E-02 | 1.9E-02 | 1 | |||
| rs1057518673 | 1.000 | 17 | 81512237 | missense variant | G/A | snv | 1 | ||||
| rs11549190 | 1.000 | 17 | 81511586 | missense variant | G/A | snv | 1 | ||||
| rs267606630 | 1.000 | 0.120 | 17 | 81511912 | missense variant | C/G;T | snv | 8.0E-06 | 1 | ||
| rs281875325 | 1.000 | 17 | 81511907 | missense variant | G/A | snv | 1 | ||||
| rs281875326 | 1.000 | 17 | 81511526 | missense variant | G/A | snv | 1 | ||||
| rs28999111 | 1.000 | 0.120 | 17 | 81512000 | missense variant | G/A | snv | 1 | |||
| rs28999112 | 1.000 | 0.120 | 17 | 81511078 | missense variant | G/A | snv | 1 | |||
| rs587780275 | 1.000 | 17 | 81511392 | missense variant | A/T | snv | 1 | ||||
| rs104894544 | 1.000 | 0.120 | 17 | 81511913 | missense variant | T/A;C | snv | 1 | |||
| rs104894546 | 1.000 | 0.120 | 17 | 81511199 | missense variant | G/A | snv | 1 | |||
| rs11549196 | 1.000 | 17 | 81511560 | missense variant | C/A;T | snv | 1 | ||||
| rs267606631 | 1.000 | 0.120 | 17 | 81511269 | missense variant | C/T | snv | 1 | |||
| rs281875327 | 1.000 | 17 | 81511382 | missense variant | G/T | snv | 1 | ||||
| rs281875328 | 1.000 | 17 | 81511230 | missense variant | G/A;T | snv | 4.0E-06 | 1 |