| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4764887 | 0.925 | 0.080 | 12 | 102430122 | intron variant | G/A | snv | 2.2E-02 | 2 | ||
| rs745410279 | 0.925 | 0.200 | 12 | 102478498 | missense variant | T/C | snv | 4.1E-06 | 2 | ||
| rs7956547 | 0.925 | 0.120 | 12 | 102465038 | intron variant | T/C | snv | 0.25 | 2 | ||
| rs978458 | 0.925 | 0.120 | 12 | 102408461 | intron variant | T/C | snv | 0.69 | 2 | ||
| rs6219 | 1.000 | 0.080 | 12 | 102396414 | 3 prime UTR variant | C/T | snv | 8.9E-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 | ||
| rs587779350 | 1.000 | 0.120 | 12 | 102419619 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs748799635 | 1.000 | 0.080 | 12 | 102475727 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs749124997 | 1.000 | 0.040 | 12 | 102402539 | missense variant | C/T | snv | 4.0E-06 | 1 | ||
| rs776234219 | 1.000 | 0.040 | 12 | 102419531 | missense variant | G/A | snv | 1.6E-05 | 3.5E-05 | 1 |