| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2353033 | 1.000 | 0.040 | 16 | 89319153 | intron variant | C/T | snv | 0.51 | 2 | ||
| rs291671 | 1.000 | 0.040 | 20 | 33363039 | intron variant | G/A | snv | 0.92 | 2 | ||
| rs4238833 | 1.000 | 0.040 | 16 | 89984281 | intron variant | G/T | snv | 0.60 | 2 | ||
| rs4911442 | 1.000 | 0.040 | 20 | 34767243 | intron variant | G/A | snv | 0.93 | 2 | ||
| rs62068372 | 0.925 | 0.080 | 16 | 89718699 | intron variant | T/C;G | snv | 2 | |||
| rs6431588 | 0.925 | 0.040 | 2 | 238185147 | intron variant | T/C;G | snv | 0.86 | 0.85 | 2 | |
| rs6684439 | 0.925 | 0.080 | 1 | 154423363 | intron variant | C/A;T | snv | 2 | |||
| rs738322 | 0.925 | 0.040 | 22 | 38172999 | intron variant | A/G | snv | 0.52 | 2 | ||
| rs7944031 | 0.925 | 0.080 | 11 | 12907573 | intron variant | A/G | snv | 0.21 | 2 | ||
| rs869330 | 0.925 | 0.080 | 9 | 21804618 | intron variant | A/G | snv | 0.62 | 2 | ||
| rs10231520 | 1.000 | 0.040 | 7 | 20742471 | intron variant | C/T | snv | 0.29 | 1 | ||
| rs10515789 | 1.000 | 0.040 | 5 | 159079407 | intron variant | T/G | snv | 0.11 | 1 | ||
| rs10852628 | 1.000 | 0.040 | 16 | 90013519 | intron variant | C/A;T | snv | 1 | |||
| rs1351383 | 1.000 | 0.040 | 6 | 32854492 | intron variant | A/C | snv | 0.43 | 1 | ||
| rs1639679 | 1.000 | 0.040 | 7 | 140778454 | intron variant | G/T | snv | 9.8E-02 | 1 | ||
| rs17305657 | 1.000 | 0.040 | 20 | 33218782 | intron variant | T/C | snv | 5.2E-02 | 1 | ||
| rs17817117 | 1.000 | 0.040 | 7 | 20685203 | intron variant | G/C | snv | 0.29 | 1 | ||
| rs187843643 | 1.000 | 0.040 | 5 | 17453974 | intron variant | C/T | snv | 3.9E-03 | 1 | ||
| rs201131773 | 1.000 | 0.040 | 9 | 21805207 | intron variant | -/AC | delins | 1 | |||
| rs2237028 | 1.000 | 0.040 | 4 | 54670209 | intron variant | T/G | snv | 0.44 | 1 | ||
| rs228437 | 1.000 | 0.040 | 6 | 134577318 | intron variant | C/A;G;T | snv | 1 | |||
| rs2733832 | 1.000 | 0.040 | 9 | 12704725 | intron variant | C/A;G;T | snv | 8.0E-06; 0.45 | 1 | ||
| rs2981096 | 1.000 | 0.040 | 8 | 73027927 | intron variant | A/G | snv | 3.1E-02 | 1 | ||
| rs3219090 | 1.000 | 0.040 | 1 | 226376990 | intron variant | T/C | snv | 0.58 | 1 | ||
| rs35390 | 1.000 | 0.040 | 5 | 33955221 | intron variant | C/A | snv | 0.81 | 1 |