| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11790131 | 0.882 | 0.080 | 9 | 19469848 | intergenic variant | G/A;T | snv | 6 | |||
| rs143633948 | 0.882 | 0.080 | 6 | 131504454 | intron variant | G/A;C | snv | 6 | |||
| rs35467001 | 0.882 | 0.080 | 17 | 73383923 | missense variant | G/A | snv | 5.3E-02 | 6.3E-02 | 6 | |
| rs35897606 | 0.882 | 0.080 | 11 | 33436311 | intron variant | A/G | snv | 4.4E-02 | 6 | ||
| rs73084982 | 0.882 | 0.080 | 20 | 3430406 | intergenic variant | G/A | snv | 3.5E-02 | 6 | ||
| rs73132848 | 0.882 | 0.080 | 3 | 8764738 | intron variant | G/A | snv | 9.3E-02 | 6 | ||
| rs79709413 | 0.882 | 0.080 | 13 | 24740488 | upstream gene variant | G/T | snv | 4.7E-02 | 6 | ||
| rs669260 | 0.851 | 0.080 | 9 | 32503442 | intron variant | T/A;C | snv | 4 | |||
| rs11881222 | 0.925 | 0.080 | 19 | 39244283 | intron variant | A/G | snv | 0.30 | 3 | ||
| rs41279633 | 1.000 | 0.080 | 7 | 44541277 | 5 prime UTR variant | G/A;T | snv | 0.12 | 3 | ||
| rs7248668 | 0.925 | 0.080 | 19 | 39253181 | upstream gene variant | G/A | snv | 0.16 | 3 | ||
| rs730775 | 1.000 | 0.080 | 6 | 44264337 | intron variant | A/G | snv | 0.36 | 3 | ||
| rs10903035 | 1.000 | 0.080 | 1 | 24155450 | 3 prime UTR variant | G/A | snv | 0.63 | 2 | ||
| rs111200466 | 1.000 | 0.080 | 4 | 153684312 | 5 prime UTR variant | CGGCTGCTCGGCGTTCTCTCAGG/- | delins | 0.17 | 2 | ||
| rs1297986 | 1.000 | 0.080 | 3 | 107912675 | intron variant | A/G | snv | 2 | |||
| rs147257424 | 0.925 | 0.080 | 1 | 11801299 | missense variant | C/A;G;T | snv | 1.2E-05; 1.2E-05 | 2 | ||
| rs1480480967 | 1.000 | 0.080 | 9 | 21367884 | missense variant | C/T | snv | 4.0E-06 | 2 | ||
| rs2857009 | 1.000 | 0.080 | 6 | 32051969 | intron variant | G/C | snv | 0.25 | 2 | ||
| rs2978048 | 1.000 | 0.080 | 8 | 133603893 | intergenic variant | T/C;G | snv | 5.2E-02 | 2 | ||
| rs377155886 | 1.000 | 0.080 | 19 | 39247213 | missense variant | T/C | snv | 1.6E-03 | 2 | ||
| rs4803221 | 1.000 | 0.080 | 19 | 39248489 | missense variant | C/G | snv | 0.17 | 0.21 | 2 | |
| rs62120527 | 1.000 | 0.080 | 19 | 39243712 | missense variant | C/T | snv | 1.3E-02 | 1.2E-02 | 2 | |
| rs7262634 | 1.000 | 0.080 | 20 | 47205635 | downstream gene variant | T/C | snv | 8.6E-02 | 2 | ||
| rs854625 | 1.000 | 0.080 | 17 | 36001422 | missense variant | G/A;T | snv | 2 | |||
| rs1013151 | 1.000 | 0.080 | X | 12914412 | intron variant | C/T | snv | 0.51 | 1 |