| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs138449918 | 0.882 | 0.040 | 2 | 39936810 | intron variant | AT/-;ATAT | delins | 3 | |||
| rs75847378 | 1.000 | 0.080 | 2 | 39954377 | intron variant | G/A | snv | 8.3E-02 | 1 | ||
| rs887994 | 1.000 | 0.040 | 2 | 39883135 | intron variant | C/T | snv | 0.35 | 1 | ||
| rs11901530 | 1.000 | 0.040 | 2 | 39884239 | intron variant | T/G | snv | 0.52 | 1 | ||
| rs6721181 | 1.000 | 0.080 | 2 | 39888556 | intron variant | C/T | snv | 2.2E-02 | 1 | ||
| rs6544273 | 2 | 39952065 | intron variant | C/T | snv | 0.58 | 1 | ||||
| rs13011737 | 1.000 | 0.040 | 2 | 39839482 | intron variant | G/A | snv | 0.33 | 1 | ||
| rs985060 | 2 | 40057790 | intron variant | G/A;T | snv | 1 | |||||
| rs10185199 | 2 | 40055062 | intron variant | G/A | snv | 0.29 | 1 | ||||
| rs374153 | 2 | 40155572 | intron variant | C/G;T | snv | 1 | |||||
| rs6544311 | 2 | 40126137 | intron variant | A/C | snv | 0.57 | 1 | ||||
| rs404005 | 1.000 | 0.160 | 2 | 40168938 | intron variant | C/T | snv | 0.59 | 1 | ||
| rs1641457 | 2 | 40194850 | intron variant | T/A;C;G | snv | 1 |