| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1345365 | 1.000 | 0.120 | 7 | 37161008 | intron variant | G/A | snv | 0.61 | 1 | ||
| rs140407862 | 1.000 | 0.120 | 4 | 6301015 | missense variant | A/G | snv | 4.4E-05 | 1.0E-04 | 1 | |
| rs1476046 | 1.000 | 0.120 | 6 | 12292988 | intron variant | G/A | snv | 0.22 | 1 | ||
| rs16996381 | 1.000 | 0.120 | 22 | 36115231 | intergenic variant | G/A | snv | 0.31 | 1 | ||
| rs17297207 | 1.000 | 0.120 | 16 | 69609450 | intron variant | A/G | snv | 5.9E-02 | 1 | ||
| rs17471 | 1.000 | 0.120 | 3 | 120098826 | non coding transcript exon variant | A/T | snv | 6.3E-02 | 1 | ||
| rs17809399 | 1.000 | 0.120 | 22 | 33861145 | intron variant | G/A | snv | 0.21 | 1 | ||
| rs1866813 | 1.000 | 0.120 | 3 | 137083096 | intergenic variant | A/C | snv | 0.14 | 1 | ||
| rs2346061 | 1.000 | 0.120 | 18 | 74533297 | upstream gene variant | C/A | snv | 0.71 | 1 | ||
| rs2780902 | 1.000 | 0.120 | 1 | 64863417 | intron variant | C/T | snv | 0.35 | 1 | ||
| rs304029 | 1.000 | 0.120 | 3 | 4504140 | intron variant | A/C | snv | 0.35 | 1 | ||
| rs334543 | 1.000 | 0.120 | 3 | 120113774 | intron variant | C/A | snv | 0.74 | 1 | ||
| rs3765156 | 1.000 | 0.120 | 1 | 204455900 | synonymous variant | G/A | snv | 0.19 | 0.15 | 1 | |
| rs3807337 | 1.000 | 0.120 | 7 | 134779071 | intron variant | A/G;T | snv | 1 | |||
| rs39075 | 1.000 | 0.120 | 7 | 29237076 | intron variant | G/A | snv | 0.41 | 1 | ||
| rs4366 | 1.000 | 0.120 | 17 | 63498094 | 3 prime UTR variant | CT/-;CTCT | delins | 1 | |||
| rs4667466 | 1.000 | 0.120 | 2 | 162832637 | intron variant | T/C | snv | 0.52 | 1 | ||
| rs4820043 | 1.000 | 0.120 | 22 | 31251108 | intron variant | A/G;T | snv | 1 | |||
| rs5749286 | 1.000 | 0.120 | 22 | 31504373 | intron variant | C/A;T | snv | 1 | |||
| rs5749682 | 1.000 | 0.120 | 22 | 33852326 | intron variant | C/A | snv | 0.17 | 1 | ||
| rs5750250 | 1.000 | 0.120 | 22 | 36312438 | intron variant | G/A;T | snv | 1 | |||
| rs6499323 | 1.000 | 0.120 | 16 | 70590580 | intron variant | A/G | snv | 0.23 | 1 | ||
| rs6930576 | 1.000 | 0.120 | 6 | 148383818 | intron variant | G/A | snv | 0.36 | 1 | ||
| rs735853 | 1.000 | 0.120 | 22 | 36283169 | intron variant | C/G | snv | 0.34 | 1 | ||
| rs7577 | 1.000 | 0.120 | 18 | 74521112 | 3 prime UTR variant | T/A;C;G | snv | 0.21 | 1 |