| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs678741 | 0.851 | 0.200 | 10 | 101237824 | intron variant | G/A | snv | 0.51 | 4 | ||
| rs1322331 | 0.925 | 0.200 | 10 | 101226832 | 3 prime UTR variant | A/C | snv | 0.50 | 2 | ||
| rs1322332 | 1.000 | 0.040 | 10 | 101222891 | downstream gene variant | T/C | snv | 0.50 | 1 | ||
| rs6570507 | 0.827 | 0.240 | 6 | 142358435 | intron variant | G/A | snv | 0.47 | 13 | ||
| rs11598177 | 1.000 | 0.040 | 10 | 101220399 | regulatory region variant | T/C | snv | 0.47 | 1 | ||
| rs1568097 | 1.000 | 0.040 | 3 | 138468 | intron variant | T/C | snv | 0.42 | 1 | ||
| rs1400180 | 1.000 | 0.040 | 3 | 129285 | intron variant | T/G | snv | 0.37 | 1 | ||
| rs9819101 | 1.000 | 0.040 | 3 | 124824 | intron variant | G/A;C | snv | 0.35 | 1 | ||
| rs4684051 | 1.000 | 0.040 | 3 | 136842 | intron variant | A/G | snv | 0.34 | 1 | ||
| rs1588962 | 1.000 | 0.040 | 3 | 142352 | intron variant | T/C | snv | 0.32 | 1 | ||
| rs1878169 | 1.000 | 0.040 | 3 | 123429 | intron variant | A/T | snv | 0.32 | 1 | ||
| rs965084 | 1.000 | 0.040 | 3 | 125415 | intron variant | G/C | snv | 0.31 | 1 | ||
| rs7639674 | 1.000 | 0.040 | 3 | 130837 | non coding transcript exon variant | A/T | snv | 0.31 | 1 | ||
| rs10510181 | 0.882 | 0.200 | 3 | 149364 | intron variant | G/A | snv | 0.31 | 4 | ||
| rs12432472 | 1.000 | 0.040 | 14 | 26807959 | intron variant | A/C | snv | 0.25 | 1 | ||
| rs12432469 | 1.000 | 0.040 | 14 | 26807946 | intron variant | A/G | snv | 0.24 | 1 | ||
| rs1407409 | 1.000 | 0.040 | 10 | 101225650 | upstream gene variant | T/C | snv | 0.22 | 1 | ||
| rs1322330 | 1.000 | 0.040 | 10 | 101231902 | intron variant | A/G | snv | 0.22 | 1 | ||
| rs2281894 | 1.000 | 0.040 | 1 | 109267922 | synonymous variant | C/A | snv | 0.22 | 0.17 | 1 | |
| rs76319884 | 1.000 | 0.040 | 10 | 101216249 | intergenic variant | C/G | snv | 8.8E-02 | 1 | ||
| rs7914775 | 1.000 | 0.040 | 10 | 101216904 | intergenic variant | C/T | snv | 8.8E-02 | 1 | ||
| rs2070074 | 0.742 | 0.360 | 9 | 34649445 | missense variant | A/G | snv | 9.2E-02 | 7.4E-02 | 12 | |
| rs200590764 | 1.000 | 0.040 | 10 | 101216904 | intergenic variant | -/T | delins | 6.6E-03 | 1 | ||
| rs557849165 | 0.776 | 0.160 | 17 | 10656089 | splice donor variant | C/T | snv | 1.2E-03 | 9 | ||
| rs140119177 | 0.851 | 0.160 | 9 | 93447639 | missense variant | G/A | snv | 6.8E-05 | 2.2E-04 | 7 |