Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11591147 | 0.677 | 0.360 | 1 | 55039974 | missense variant | G/A;T | snv | 1.2E-02 | 28 | ||
| rs505151 | 0.732 | 0.360 | 1 | 55063514 | missense variant | G/A | snv | 0.95 | 0.90 | 18 | |
| rs562556 | 0.827 | 0.280 | 1 | 55058564 | missense variant | G/A | snv | 0.86 | 0.83 | 8 | |
| rs67608943 | 0.851 | 0.080 | 1 | 55046549 | stop gained | C/G;T | snv | 1.9E-04 | 8 | ||
| rs17111503 | 0.925 | 0.160 | 1 | 55037775 | upstream gene variant | A/G | snv | 0.22 | 7 | ||
| rs28362261 | 0.851 | 0.160 | 1 | 55058129 | missense variant | A/G | snv | 1.2E-03 | 4.8E-03 | 6 | |
| rs28362286 | 0.851 | 0.080 | 1 | 55063542 | stop gained | C/A;T | snv | 5.6E-04 | 6 | ||
| rs11206517 | 1.000 | 0.120 | 1 | 55060755 | intron variant | T/C;G | snv | 4 | |||
| rs2479409 | 1.000 | 0.040 | 1 | 55038977 | upstream gene variant | G/A | snv | 0.66 | 4 | ||
| rs10888898 | 1 | 55050835 | intron variant | A/G | snv | 0.59 | 3 | ||||
| rs11206514 | 1 | 55050331 | intron variant | C/A | snv | 0.52 | 3 | ||||
| rs1165287 | 1 | 55054539 | intron variant | G/A | snv | 0.52 | 3 | ||||
| rs11806638 | 1 | 55052487 | intron variant | C/A;G | snv | 3 | |||||
| rs2479410 | 1 | 55040188 | intron variant | G/A | snv | 0.29 | 3 | ||||
| rs2479413 | 1 | 55053009 | intron variant | C/T | snv | 0.38 | 3 | ||||
| rs2495477 | 1 | 55052794 | splice region variant | A/G | snv | 0.42 | 0.49 | 3 | |||
| rs28362263 | 1.000 | 0.080 | 1 | 55058182 | missense variant | G/A;C | snv | 7.2E-03 | 3 | ||
| rs471705 | 1 | 55055569 | intron variant | T/A;G | snv | 0.51 | 3 | ||||
| rs499883 | 1 | 55053501 | intron variant | G/A;C | snv | 3 | |||||
| rs557435 | 1 | 55055191 | intron variant | A/G | snv | 0.79 | 3 | ||||
| rs565436 | 1 | 55058928 | intron variant | G/A;C | snv | 0.71 | 3 | ||||
| rs634272 | 1 | 55054592 | intron variant | T/C | snv | 0.72 | 3 | ||||
| rs644000 | 1 | 55046322 | intron variant | A/G | snv | 0.30 | 3 | ||||
| rs11800231 | 1 | 55052267 | non coding transcript exon variant | G/A;T | snv | 5.2E-02; 4.0E-06 | 2 | ||||
| rs151193009 | 1 | 55043912 | missense variant | C/T | snv | 7.4E-04 | 1.5E-04 | 2 |