| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2292239 | 0.742 | 0.480 | 12 | 56088396 | intron variant | T/G | snv | 0.65 | 13 | ||
| rs11171739 | 0.807 | 0.320 | 12 | 56076841 | 5 prime UTR variant | C/T | snv | 0.49 | 10 | ||
| rs1057519893 | 0.790 | 0.160 | 12 | 56085070 | missense variant | G/A;T | snv | 9 | |||
| rs1057519891 | 0.851 | 0.160 | 12 | 56088557 | missense variant | G/A;T | snv | 4.0E-06 | 6 | ||
| rs1057519892 | 0.851 | 0.160 | 12 | 56088558 | missense variant | A/T | snv | 5 | |||
| rs1057519803 | 0.925 | 0.080 | 12 | 56088138 | missense variant | G/A | snv | 4 | |||
| rs877636 | 1.000 | 0.120 | 12 | 56086799 | intron variant | G/A | snv | 0.61 | 2 | ||
| rs3202538 | 0.925 | 0.080 | 12 | 56102447 | 3 prime UTR variant | G/T | snv | 2 | |||
| rs1057519817 | 12 | 56088073 | missense variant | C/A;G | snv | 4.0E-06 | 1 | ||||
| rs10783779 | 12 | 56098096 | intron variant | T/A;G | snv | 1 | |||||
| rs2271194 | 1.000 | 0.120 | 12 | 56083910 | splice region variant | A/T | snv | 0.63 | 0.53 | 1 | |
| rs34379766 | 12 | 56080359 | missense variant | C/A;T | snv | 4.6E-06; 4.6E-06 | 1 | ||||
| rs755855285 | 12 | 56102035 | missense variant | G/A | snv | 1.1E-04 | 1.4E-04 | 1 | |||
| rs765301443 | 1.000 | 0.080 | 12 | 56098767 | missense variant | G/A;C | snv | 8.0E-06; 1.2E-05 | 1 | ||
| rs931676601 | 12 | 56097196 | missense variant | A/G;T | snv | 1 | |||||
| rs79335261 | 1.000 | 0.080 | 12 | 56103857 | intron variant | G/A;T | snv | 1 |