| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4073 | 0.566 | 0.800 | 4 | 73740307 | upstream gene variant | A/T | snv | 0.46 | 64 | ||
| rs2227306 | 0.677 | 0.680 | 4 | 73741338 | intron variant | C/T | snv | 0.31 | 21 | ||
| rs1126647 | 0.827 | 0.160 | 4 | 73743328 | 3 prime UTR variant | A/T | snv | 0.31 | 8 | ||
| rs2227307 | 0.851 | 0.240 | 4 | 73740952 | intron variant | T/G | snv | 0.45 | 6 | ||
| rs2227532 | 0.882 | 0.120 | 4 | 73739815 | upstream gene variant | T/C | snv | 2.9E-02 | 3 | ||
| rs2227543 | 1.000 | 0.120 | 4 | 73742193 | 3 prime UTR variant | C/T | snv | 0.32 | 1 | ||
| rs2227544 | 4 | 73742906 | 3 prime UTR variant | G/A | snv | 4.4E-03 | 1 | ||||
| rs373821605 | 1.000 | 0.120 | 4 | 73741652 | missense variant | C/T | snv | 2.1E-05 | 1 | ||
| rs774766411 | 1.000 | 0.040 | 4 | 73741625 | missense variant | A/G | snv | 1.2E-05 | 1 | ||
| rs780209935 | 1.000 | 0.040 | 4 | 73742000 | stop gained | G/A | snv | 8.0E-06 | 1 |