| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2851447 | 1.000 | 0.040 | 12 | 123180566 | intron variant | G/C | snv | 0.59 | 2 | ||
| rs1615350 | 1.000 | 0.040 | 12 | 123165788 | intron variant | C/T | snv | 0.58 | 2 | ||
| rs10654220 | 1.000 | 0.040 | 12 | 123218875 | intron variant | -/TGT;TGTTGT | delins | 2 | |||
| rs1727313 | 1.000 | 0.080 | 12 | 123156306 | 3 prime UTR variant | C/G | snv | 0.84 | 1 | ||
| rs1716162 | 12 | 123157991 | intron variant | T/A | snv | 0.63 | 1 | ||||
| rs2851437 | 12 | 123169045 | intron variant | C/A;T | snv | 1 | |||||
| rs1790100 | 1.000 | 0.080 | 12 | 123172178 | intron variant | G/T | snv | 0.63 | 1 | ||
| rs61041384 | 1.000 | 0.040 | 12 | 123159496 | intron variant | T/C | snv | 4.5E-02 | 1 | ||
| rs2102949 | 1.000 | 0.040 | 12 | 123192216 | intron variant | G/A | snv | 0.59 | 1 | ||
| rs2695478 | 12 | 123204974 | intron variant | C/T | snv | 0.84 | 1 | ||||
| rs1790105 | 12 | 123183403 | intron variant | T/A;C | snv | 1 | |||||
| rs2851436 | 12 | 123182807 | intron variant | G/T | snv | 0.64 | 1 |