| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11209290 | 1.000 | 0.040 | 1 | 68405344 | intergenic variant | G/A | snv | 6.7E-02 | 1 | ||
| rs11240572 | 1.000 | 0.040 | 1 | 205838885 | intron variant | C/A;T | snv | 1 | |||
| rs11248051 | 1.000 | 0.040 | 4 | 864544 | intron variant | C/G;T | snv | 1 | |||
| rs11248060 | 1.000 | 0.040 | 4 | 970571 | intron variant | C/T | snv | 9.3E-02 | 1 | ||
| rs11564273 | 1.000 | 0.040 | 12 | 40204350 | intron variant | T/G | snv | 6.5E-02 | 1 | ||
| rs11711441 | 1.000 | 0.040 | 3 | 183103487 | intron variant | G/A | snv | 0.12 | 1 | ||
| rs11724635 | 0.925 | 0.080 | 4 | 15735478 | intron variant | C/A;G | snv | 0.43 | 1 | ||
| rs11724804 | 0.882 | 0.160 | 4 | 971991 | intron variant | G/A | snv | 0.43 | 1 | ||
| rs11865038 | 1.000 | 0.040 | 16 | 31083850 | 3 prime UTR variant | C/T | snv | 0.42 | 0.46 | 1 | |
| rs11868035 | 0.763 | 0.200 | 17 | 17811787 | splice region variant | G/A | snv | 0.45 | 0.33 | 1 | |
| rs11931074 | 0.851 | 0.080 | 4 | 89718364 | intron variant | G/A;C;T | snv | 1 | |||
| rs11931532 | 1.000 | 0.040 | 4 | 15724143 | intron variant | T/C | snv | 0.13 | 1 | ||
| rs12063142 | 1.000 | 0.040 | 1 | 18813023 | intergenic variant | C/T | snv | 0.28 | 1 | ||
| rs12069733 | 1.000 | 0.040 | 1 | 43475837 | TF binding site variant | G/A | snv | 0.37 | 1 | ||
| rs12150390 | 1.000 | 0.040 | 17 | 45818862 | intron variant | T/C | snv | 0.14 | 1 | ||
| rs12185233 | 0.882 | 0.160 | 17 | 45846288 | missense variant | G/A;C | snv | 9.5E-05; 0.15 | 4 | ||
| rs12185235 | 0.925 | 0.120 | 17 | 45846337 | synonymous variant | C/T | snv | 0.14 | 0.14 | 3 | |
| rs12185268 | 0.851 | 0.160 | 17 | 45846317 | missense variant | A/G | snv | 0.15 | 0.14 | 3 | |
| rs1229984 | 0.570 | 0.560 | 4 | 99318162 | missense variant | T/C;G | snv | 0.90 | 6 | ||
| rs12364577 | 1.000 | 0.040 | 11 | 49685809 | intron variant | A/C | snv | 0.35 | 1 | ||
| rs12373123 | 0.882 | 0.160 | 17 | 45846707 | missense variant | T/C | snv | 0.15 | 0.14 | 4 | |
| rs12373139 | 0.925 | 0.120 | 17 | 45846764 | missense variant | G/A | snv | 0.15 | 0.14 | 4 | |
| rs12373142 | 0.851 | 0.200 | 17 | 45846834 | missense variant | C/G;T | snv | 0.15 | 4 | ||
| rs12411886 | 0.882 | 0.080 | 10 | 102925542 | intron variant | C/A | snv | 7.8E-02 | 3 | ||
| rs12413409 | 0.790 | 0.200 | 10 | 102959339 | intron variant | G/A | snv | 9.0E-02 | 6 |