| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2268388 | 0.851 | 0.200 | 12 | 109205840 | intron variant | G/A | snv | 0.14 | 6 | ||
| rs2239607 | 0.925 | 0.120 | 12 | 109209475 | intron variant | A/G | snv | 0.14 | 3 | ||
| rs104893636 | 0.882 | 0.120 | 2 | 176151875 | missense variant | A/C;T | snv | 5.2E-06; 7.9E-04 | 3 | ||
| rs2241220 | 1.000 | 0.040 | 12 | 109237224 | synonymous variant | T/A;C;G | snv | 4.0E-06; 0.83 | 2 | ||
| rs4078756 | 0.925 | 0.080 | 2 | 176139387 | non coding transcript exon variant | T/C | snv | 2.0E-02 | 2 | ||
| rs4766587 | 1.000 | 0.040 | 12 | 109247525 | intron variant | G/A | snv | 0.23 | 1 | ||
| rs6606697 | 1.000 | 0.040 | 12 | 109173915 | intron variant | A/G | snv | 0.48 | 1 |