| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs304029 | 1.000 | 0.120 | 3 | 4504140 | intron variant | A/C | snv | 0.35 | 1 | ||
| rs2780902 | 1.000 | 0.120 | 1 | 64863417 | intron variant | C/T | snv | 0.35 | 1 | ||
| rs4667466 | 1.000 | 0.120 | 2 | 162832637 | intron variant | T/C | snv | 0.52 | 1 | ||
| rs17809399 | 1.000 | 0.120 | 22 | 33861145 | intron variant | G/A | snv | 0.21 | 1 | ||
| rs5749682 | 1.000 | 0.120 | 22 | 33852326 | intron variant | C/A | snv | 0.17 | 1 | ||
| rs4820043 | 1.000 | 0.120 | 22 | 31251108 | intron variant | A/G;T | snv | 1 | |||
| rs1298908 | 1.000 | 0.120 | 10 | 80253378 | non coding transcript exon variant | C/T | snv | 0.48 | 0.53 | 1 | |
| rs17471 | 1.000 | 0.120 | 3 | 120098826 | non coding transcript exon variant | A/T | snv | 6.3E-02 | 1 | ||
| rs7639705 | 1.000 | 0.120 | 3 | 183309754 | missense variant | T/G | snv | 0.26 | 0.27 | 1 | |
| rs770917264 | 1.000 | 0.120 | 14 | 102229547 | stop gained | G/A;C | snv | 4.0E-06; 1.6E-05 | 1 | ||
| rs5750250 | 1.000 | 0.120 | 22 | 36312438 | intron variant | G/A;T | snv | 1 | |||
| rs735853 | 1.000 | 0.120 | 22 | 36283169 | intron variant | C/G | snv | 0.34 | 1 | ||
| rs11107616 | 1.000 | 0.120 | 12 | 77971000 | intron variant | T/G | snv | 0.13 | 1 | ||
| rs17297207 | 1.000 | 0.120 | 16 | 69609450 | intron variant | A/G | snv | 5.9E-02 | 1 | ||
| rs10047560 | 1.000 | 0.120 | 12 | 20452282 | intron variant | A/G | snv | 0.86 | 1 | ||
| rs3765156 | 1.000 | 0.120 | 1 | 204455900 | synonymous variant | G/A | snv | 0.19 | 0.15 | 1 | |
| rs1034589 | 1.000 | 0.120 | 22 | 31183247 | intron variant | C/T | snv | 0.79 | 1 | ||
| rs6930576 | 1.000 | 0.120 | 6 | 148383818 | intron variant | G/A | snv | 0.36 | 1 | ||
| rs11645214 | 1.000 | 0.120 | 16 | 70575084 | 3 prime UTR variant | A/G | snv | 0.39 | 1 | ||
| rs5749286 | 1.000 | 0.120 | 22 | 31504373 | intron variant | C/A;T | snv | 1 | |||
| rs13254600 | 1.000 | 0.120 | 8 | 123077286 | intron variant | C/A;G | snv | 0.28; 4.8E-06 | 1 | ||
| rs11130362 | 1.000 | 0.120 | 3 | 53231750 | non coding transcript exon variant | C/T | snv | 0.24 | 1 | ||
| rs7638459 | 1.000 | 0.120 | 3 | 142771309 | intron variant | T/C | snv | 0.35 | 1 | ||
| rs953239 | 1.000 | 0.120 | 3 | 142727363 | intron variant | A/C | snv | 0.46 | 1 | ||
| rs140407862 | 1.000 | 0.120 | 4 | 6301015 | missense variant | A/G | snv | 4.4E-05 | 1.0E-04 | 1 |