| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7956547 | 0.925 | 0.120 | 12 | 102465038 | intron variant | T/C | snv | 0.25 | 2 | ||
| rs12423791 | 0.925 | 0.040 | 12 | 102465050 | intron variant | G/C | snv | 2.8E-02 | 5 | ||
| rs745805222 | 0.790 | 0.120 | 12 | 102475722 | synonymous variant | C/T | snv | 1.2E-05 | 4.9E-05 | 7 | |
| rs748799635 | 1.000 | 0.080 | 12 | 102475727 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
| rs1239905891 | 0.925 | 0.080 | 12 | 102475786 | missense variant | G/A;T | snv | 3 | |||
| rs5742617 | 12 | 102476127 | intron variant | C/T | snv | 8.7E-03 | 1 | ||||
| rs2162679 | 0.851 | 0.240 | 12 | 102477481 | intron variant | C/G;T | snv | 6 | |||
| rs745410279 | 0.925 | 0.200 | 12 | 102478498 | missense variant | T/C | snv | 4.1E-06 | 2 | ||
| rs2288377 | 0.925 | 0.080 | 12 | 102480984 | intron variant | A/G;T | snv | 2 | |||
| rs5742612 | 0.752 | 0.440 | 12 | 102481086 | intron variant | A/G | snv | 5.6E-02 | 11 | ||
| rs35767 | 0.763 | 0.360 | 12 | 102481791 | upstream gene variant | A/C;G;T | snv | 13 |