| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs9878775 | 1.000 | 0.040 | 3 | 182942165 | 3 prime UTR variant | T/A;C | snv | 1 | |||
| rs9952724 | 1.000 | 0.040 | 18 | 48726444 | intron variant | A/C;T | snv | 1 | |||
| rs34637584 | 0.583 | 0.480 | 12 | 40340400 | missense variant | G/A | snv | 5.3E-04 | 3.6E-04 | 1 | |
| rs34778348 | 0.742 | 0.120 | 12 | 40363526 | missense variant | G/A | snv | 1.7E-03 | 5.8E-04 | 1 | |
| rs28903073 | 1.000 | 0.040 | 12 | 40259708 | intron variant | G/A | snv | 2.4E-03 | 1 | ||
| rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 10 | |
| rs34372695 | 1.000 | 0.040 | 1 | 156060246 | upstream gene variant | C/G;T | snv | 1.5E-02 | 1 | ||
| rs2070600 | 0.561 | 0.760 | 6 | 32183666 | missense variant | C/T | snv | 5.3E-02 | 3.6E-02 | 4 | |
| rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 14 | |
| rs10506095 | 1.000 | 0.040 | 12 | 32647193 | downstream gene variant | C/T | snv | 4.4E-02 | 1 | ||
| rs2046932 | 1.000 | 0.040 | 12 | 40186638 | intron variant | G/A | snv | 4.8E-02 | 1 | ||
| rs1630500 | 1.000 | 0.040 | 1 | 154882579 | intergenic variant | G/A | snv | 5.0E-02 | 1 | ||
| rs17497526 | 1.000 | 0.040 | 10 | 69820364 | intron variant | T/C | snv | 6.0E-02 | 1 | ||
| rs2275336 | 1.000 | 0.040 | 6 | 154405854 | 3 prime UTR variant | G/A | snv | 6.3E-02 | 1 | ||
| rs11564273 | 1.000 | 0.040 | 12 | 40204350 | intron variant | T/G | snv | 6.5E-02 | 1 | ||
| rs11209290 | 1.000 | 0.040 | 1 | 68405344 | intergenic variant | G/A | snv | 6.7E-02 | 1 | ||
| rs1442190 | 1.000 | 0.040 | 12 | 40971838 | 3 prime UTR variant | G/A | snv | 6.8E-02 | 1 | ||
| rs7118648 | 1.000 | 0.040 | 11 | 96375264 | intron variant | T/C;G | snv | 7.5E-02 | 1 | ||
| rs12411886 | 0.882 | 0.080 | 10 | 102925542 | intron variant | C/A | snv | 7.8E-02 | 3 | ||
| rs12645693 | 1.000 | 0.040 | 4 | 15727911 | intron variant | G/A | snv | 8.1E-02 | 1 | ||
| rs1564282 | 1.000 | 0.040 | 4 | 858525 | intron variant | C/T | snv | 8.1E-02 | 1 | ||
| rs8086137 | 1.000 | 0.040 | 18 | 31127452 | intron variant | T/C | snv | 8.7E-02 | 1 | ||
| rs3796661 | 1.000 | 0.040 | 4 | 89766356 | intron variant | C/T | snv | 8.7E-02 | 1 | ||
| rs12413409 | 0.790 | 0.200 | 10 | 102959339 | intron variant | G/A | snv | 9.0E-02 | 6 | ||
| rs11248060 | 1.000 | 0.040 | 4 | 970571 | intron variant | C/T | snv | 9.3E-02 | 1 |