| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12105421 | 1.000 | 0.040 | 2 | 102959630 | intron variant | C/T | snv | 7.8E-02 | 2 | ||
| rs12196860 | 1.000 | 0.040 | 6 | 56085576 | intron variant | G/A | snv | 0.15 | 2 | ||
| rs1959536 | 1.000 | 0.040 | 14 | 50980053 | intron variant | T/G | snv | 9.7E-02 | 2 | ||
| rs245914 | 1.000 | 0.040 | 7 | 29178543 | intron variant | G/A;T | snv | 2 | |||
| rs6081541 | 1.000 | 0.040 | 20 | 19232246 | intron variant | A/G | snv | 0.20 | 2 | ||
| rs7912580 | 1.000 | 0.040 | 10 | 62156213 | regulatory region variant | G/A | snv | 7.6E-02 | 2 |