| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11806129 | 1 | 94016821 | intron variant | A/G;T | snv | 3 | |||||
| rs12087003 | 1 | 94037627 | intron variant | A/G | snv | 6.3E-02 | 3 | ||||
| rs1801466 | 1.000 | 1 | 94010911 | missense variant | T/A | snv | 4.3E-02 | 4.1E-02 | 3 | ||
| rs61750138 | 1.000 | 1 | 94030991 | splice region variant | C/A;T | snv | 1.2E-05 | 3 | |||
| rs121909205 | 1.000 | 1 | 94120994 | missense variant | G/A;T | snv | 1.6E-05; 3.6E-05 | 2 | |||
| rs150774447 | 1.000 | 1 | 94111579 | missense variant | C/A;T | snv | 4.0E-06; 2.4E-05 | 2 | |||
| rs1553186896 | 1.000 | 1 | 94005490 | missense variant | A/C;G | snv | 2 | ||||
| rs17110922 | 1 | 94043489 | intron variant | A/T | snv | 2.5E-03 | 9.9E-03 | 2 | |||
| rs61748538 | 1.000 | 1 | 94098904 | missense variant | G/A | snv | 8.0E-06 | 1.4E-05 | 2 | ||
| rs61748552 | 1.000 | 1 | 94078611 | missense variant | G/C | snv | 8.0E-06 | 8.3E-06 | 2 | ||
| rs61750135 | 1.000 | 1 | 94031027 | missense variant | A/G | snv | 1.6E-05 | 1.4E-05 | 2 | ||
| rs61751377 | 1.000 | 1 | 94019581 | splice donor variant | C/T | snv | 2.2E-05 | 7.0E-06 | 2 | ||
| rs61753034 | 1.000 | 1 | 94007727 | missense variant | A/C | snv | 2 | ||||
| rs62642574 | 1.000 | 1 | 94024994 | missense variant | C/T | snv | 1.1E-04 | 6.3E-05 | 2 | ||
| rs62654397 | 1.000 | 1 | 94111537 | missense variant | G/A;C | snv | 8.0E-06 | 2 | |||
| rs756840095 | 1.000 | 1 | 94042797 | missense variant | G/A | snv | 2.4E-05 | 6.3E-05 | 2 | ||
| rs760549861 | 1.000 | 1 | 94014685 | missense variant | G/A | snv | 7.6E-05 | 7.0E-06 | 2 | ||
| rs1047376 | 1.000 | 1 | 94041354 | missense variant | A/G;T | snv | 4.0E-06 | 1 | |||
| rs1064793014 | 1 | 94007707 | missense variant | T/C | snv | 1 | |||||
| rs121909204 | 1.000 | 1 | 94043443 | missense variant | G/A | snv | 1 | ||||
| rs121909207 | 1.000 | 1 | 94014665 | missense variant | G/A;C | snv | 1.1E-04 | 1 | |||
| rs1297857869 | 1.000 | 1 | 94011330 | missense variant | A/G | snv | 4.0E-06 | 1 | |||
| rs1356104318 | 1 | 94098850 | stop gained | G/A;C | snv | 4.0E-06 | 1 | ||||
| rs137866734 | 1 | 94074274 | intron variant | C/T | snv | 6.8E-03 | 1 | ||||
| rs140482171 | 1.000 | 1 | 94077712 | missense variant | C/T | snv | 7.8E-04 | 4.1E-04 | 1 |