| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs386834126 | 1.000 | 0.120 | 8 | 1771374 | missense variant | T/G | snv | 1 | |||
| rs386834127 | 1.000 | 0.120 | 8 | 1771469 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs386834128 | 1.000 | 0.120 | 8 | 1771518 | missense variant | C/A;T | snv | 1 | |||
| rs386834129 | 1.000 | 0.120 | 8 | 1771100 | missense variant | C/A;G;T | snv | 2.0E-05; 4.0E-06 | 1 | ||
| rs386834130 | 1.000 | 0.120 | 8 | 1771527 | missense variant | A/G | snv | 8.0E-06 | 7.0E-06 | 1 | |
| rs386834132 | 1.000 | 0.120 | 8 | 1780265 | frameshift variant | CT/- | delins | 1 | |||
| rs386834133 | 1.000 | 0.120 | 8 | 1780287 | missense variant | A/G | snv | 1 | |||
| rs386834134 | 1.000 | 0.120 | 8 | 1780317 | missense variant | G/A;T | snv | 8.0E-06; 4.0E-06 | 1 | ||
| rs386834135 | 1.000 | 0.120 | 8 | 1780339 | inframe deletion | TGG/- | delins | 1 | |||
| rs386834136 | 1.000 | 0.120 | 8 | 1780367 | missense variant | G/A | snv | 4.4E-05 | 3.5E-05 | 1 | |
| rs386834138 | 1.000 | 0.120 | 8 | 1780472 | missense variant | C/G | snv | 1 | |||
| rs386834139 | 1.000 | 0.120 | 8 | 1771142 | frameshift variant | G/- | del | 1 | |||
| rs554042394 | 1.000 | 0.120 | 8 | 1771452 | stop gained | T/A;G | snv | 1.2E-05 | 1 | ||
| rs746397087 | 1.000 | 0.120 | 8 | 1780469 | stop gained | C/T | snv | 4.0E-06 | 1 | ||
| rs746645358 | 1.000 | 0.120 | 8 | 1780415 | missense variant | G/A | snv | 2.0E-05 | 7.0E-06 | 1 | |
| rs756267448 | 1.000 | 0.120 | 8 | 1771598 | splice donor variant | G/T | snv | 4.0E-06 | 2.1E-05 | 1 | |
| rs759830733 | 1.000 | 0.120 | 8 | 1771337 | stop gained | A/T | snv | 7.0E-06 | 1 | ||
| rs781166361 | 1.000 | 0.120 | 8 | 1780326 | missense variant | T/G | snv | 4.0E-06 | 1 |