| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs79105258 | 12 | 111280427 | intron variant | C/A;T | snv | 23 | |||||
| rs2157999 | 1.000 | 12 | 111266635 | intron variant | G/A | snv | 8.1E-02 | 5 | |||
| rs1265564 | 1.000 | 0.120 | 12 | 111270654 | non coding transcript exon variant | A/C | snv | 0.30 | 4 | ||
| rs4766566 | 0.851 | 0.200 | 12 | 111269073 | intron variant | C/T | snv | 0.42 | 4 | ||
| rs147032946 | 12 | 111151263 | intron variant | C/A;T | snv | 2 | |||||
| rs886126 | 1.000 | 0.040 | 12 | 111241410 | intron variant | C/T | snv | 0.34 | 1 | ||
| rs2339717 | 12 | 111258724 | intron variant | T/C | snv | 0.45 | 1 | ||||
| rs76721774 | 12 | 111268872 | intron variant | A/C | snv | 1.1E-02 | 1 | ||||
| rs6490061 | 0.925 | 0.120 | 12 | 111335541 | intron variant | T/C | snv | 0.30 | 1 | ||
| rs11830764 | 12 | 111077216 | intron variant | G/A;C;T | snv | 1 |