| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs587779350 | 1.000 | 0.120 | 12 | 102419619 | missense variant | G/A | snv | 7.0E-06 | 1 | ||
| rs35767 | 0.763 | 0.360 | 12 | 102481791 | upstream gene variant | A/C;G;T | snv | 13 | |||
| rs2162679 | 0.851 | 0.240 | 12 | 102477481 | intron variant | C/G;T | snv | 6 | |||
| rs1239905891 | 0.925 | 0.080 | 12 | 102475786 | missense variant | G/A;T | snv | 3 | |||
| rs2288377 | 0.925 | 0.080 | 12 | 102480984 | intron variant | A/G;T | snv | 2 | |||
| rs745410279 | 0.925 | 0.200 | 12 | 102478498 | missense variant | T/C | snv | 4.1E-06 | 2 | ||
| rs121912430 | 1.000 | 0.120 | 12 | 102419637 | missense variant | C/T | snv | 1 | |||
| rs5742663 | 12 | 102430212 | intron variant | T/A;G | snv | 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 | ||
| rs9308315 | 12 | 102410115 | intron variant | A/C;T | snv | 1 |