| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1222174664 | 0.827 | 0.280 | 5 | 102477801 | missense variant | G/A | snv | 8.0E-06 | 7.0E-06 | 5 | |
| rs28362491 | 0.592 | 0.720 | 4 | 102500998 | non coding transcript exon variant | ATTG/- | delins | 56 | |||
| rs2276109 | 0.701 | 0.440 | 11 | 102875061 | upstream gene variant | T/C | snv | 9.2E-02 | 18 | ||
| rs567798234 | 0.851 | 0.120 | 1 | 109625326 | missense variant | C/T | snv | 4.1E-06 | 7.0E-06 | 5 | |
| rs1860561 | 0.851 | 0.080 | 12 | 110345436 | intron variant | G/A | snv | 0.19 | 5 | ||
| rs9885413 | 0.925 | 0.040 | 5 | 110840429 | intergenic variant | G/T | snv | 0.19 | 2 | ||
| rs1544223 | 1.000 | 0.040 | 1 | 111503935 | intron variant | C/T | snv | 0.72 | 1 | ||
| rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
| rs737337 | 0.925 | 0.040 | 19 | 11236817 | synonymous variant | T/C | snv | 0.15 | 0.20 | 6 | |
| rs397507549 | 0.742 | 0.240 | 12 | 112489104 | missense variant | C/A;G | snv | 13 | |||
| rs1801252 | 0.724 | 0.320 | 10 | 114044277 | missense variant | A/G | snv | 0.15 | 0.17 | 17 | |
| rs1801253 | 0.683 | 0.440 | 10 | 114045297 | missense variant | G/C | snv | 0.74 | 0.69 | 34 | |
| rs749303395 | 0.882 | 0.040 | 1 | 114680329 | missense variant | G/A;C | snv | 8.0E-06; 4.0E-06 | 3 | ||
| rs7521023 | 1.000 | 0.040 | 1 | 115700759 | 3 prime UTR variant | G/A | snv | 0.64 | 2 | ||
| rs6684209 | 1.000 | 0.040 | 1 | 115707991 | intron variant | C/T | snv | 0.17 | 2 | ||
| rs740363 | 0.851 | 0.080 | 10 | 116816095 | intron variant | G/A | snv | 0.40 | 5 | ||
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs198358 | 0.925 | 0.040 | 1 | 11844019 | 3 prime UTR variant | T/C | snv | 0.32 | 4 | ||
| rs5068 | 0.776 | 0.160 | 1 | 11845917 | 3 prime UTR variant | A/G;T | snv | 13 | |||
| rs111033560 | 0.807 | 0.040 | 6 | 118559037 | stop gained | T/G | snv | 1.6E-05 | 9 | ||
| rs2230345 | 0.807 | 0.160 | 10 | 119326585 | missense variant | A/T | snv | 3.8E-02 | 9.0E-02 | 6 | |
| rs397516881 | 0.827 | 0.120 | 10 | 119676917 | missense variant | G/A | snv | 7 | |||
| rs1061622 | 0.633 | 0.760 | 1 | 12192898 | missense variant | T/G | snv | 0.22 | 0.22 | 33 | |
| rs5370 | 0.630 | 0.520 | 6 | 12296022 | missense variant | G/T | snv | 0.23 | 0.21 | 37 | |
| rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 131 |