| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs34856868 | 1 | 92088726 | missense variant | G/A | snv | 2.0E-02 | 2.0E-02 | 1 | |||
| rs7533077 | 1.000 | 0.040 | 1 | 92118962 | intron variant | A/G;T | snv | 1 | |||
| rs2093879 | 1.000 | 0.040 | 1 | 92120274 | intron variant | C/G | snv | 0.59 | 1 | ||
| rs2893200 | 1.000 | 0.040 | 1 | 92142472 | intron variant | G/A | snv | 0.62 | 1 | ||
| rs563113 | 1.000 | 0.040 | 1 | 92143295 | intron variant | G/T | snv | 0.70 | 1 | ||
| rs492164 | 1.000 | 0.040 | 1 | 92146450 | intron variant | G/A | snv | 0.72 | 1 | ||
| rs4437922 | 1.000 | 0.040 | 1 | 92116261 | intron variant | T/C | snv | 0.59 | 1 | ||
| rs10875204 | 1.000 | 0.040 | 1 | 92114118 | intron variant | G/A | snv | 0.59 | 1 | ||
| rs519623 | 1.000 | 0.040 | 1 | 92152766 | intron variant | G/C;T | snv | 1 |