| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs5742626 | 12 | 102464131 | intron variant | T/C | snv | 2.3E-02 | 3 | ||||
| rs5742692 | 12 | 102405820 | intron variant | A/G | snv | 6.6E-02 | 2 | ||||
| rs121912430 | 1.000 | 0.120 | 12 | 102419637 | missense variant | C/T | snv | 1 | |||
| rs5742629 | 1.000 | 0.040 | 12 | 102463485 | non coding transcript exon variant | T/C | snv | 0.32 | 1 | ||
| rs5742643 | 12 | 102444085 | intron variant | T/C | snv | 0.76 | 1 | ||||
| rs5742683 | 12 | 102419939 | intron variant | A/G | snv | 3.3E-02 | 1 | ||||
| rs587779350 | 1.000 | 0.120 | 12 | 102419619 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs749124997 | 1.000 | 0.040 | 12 | 102402539 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs9308315 | 12 | 102410115 | intron variant | A/C;T | snv | 1 | |||||
| rs5742612 | 0.752 | 0.440 | 12 | 102481086 | intron variant | A/G | snv | 5.6E-02 | 11 | ||
| rs2288377 | 0.925 | 0.080 | 12 | 102480984 | intron variant | A/G;T | snv | 2 |