| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs964184 | 0.716 | 0.440 | 11 | 116778201 | 3 prime UTR variant | G/C | snv | 0.82 | 12 | ||
| rs2266788 | 0.763 | 0.440 | 11 | 116789970 | 3 prime UTR variant | G/A | snv | 0.93 | 7 | ||
| rs6589566 | 0.882 | 0.080 | 11 | 116781707 | intron variant | G/A;C;T | snv | 7 | |||
| rs2075290 | 0.882 | 0.160 | 11 | 116782580 | intron variant | C/G;T | snv | 7 | |||
| rs12286037 | 1.000 | 0.040 | 11 | 116781491 | intron variant | C/T | snv | 0.11 | 6 | ||
| rs2072560 | 11 | 116791110 | missense variant | T/C | snv | 0.89 | 0.94 | 5 | |||
| rs12285095 | 11 | 116787315 | non coding transcript exon variant | T/G | snv | 9.8E-02 | 4 | ||||
| rs3741298 | 11 | 116786845 | intron variant | C/T | snv | 0.73 | 3 | ||||
| rs11823543 | 11 | 116778419 | 3 prime UTR variant | G/A | snv | 0.11 | 2 | ||||
| rs2160669 | 1.000 | 0.040 | 11 | 116776891 | 3 prime UTR variant | C/T | snv | 0.92 | 2 | ||
| rs619054 | 11 | 116790097 | 3 prime UTR variant | G/A | snv | 0.19 | 0.19 | 1 | |||
| rs35120633 | 11 | 116784884 | missense variant | G/A;C | snv | 6.6E-02; 8.0E-06 | 1 | ||||
| rs4417316 | 11 | 116781585 | intron variant | C/T | snv | 9.0E-02 | 1 | ||||
| rs603446 | 1.000 | 0.040 | 11 | 116783719 | intron variant | C/T | snv | 0.33 | 1 | ||
| rs618923 | 11 | 116783443 | intron variant | A/G | snv | 0.20 | 1 | ||||
| rs7926960 | 11 | 116783370 | intron variant | A/C | snv | 1.5E-02 | 1 | ||||
| rs10750096 | 11 | 116786072 | intron variant | C/A | snv | 0.92 | 1 | ||||
| rs11604424 | 11 | 116780399 | intron variant | C/G;T | snv | 1 | |||||
| rs17120029 | 11 | 116779402 | intron variant | C/T | snv | 0.11 | 1 | ||||
| rs3741297 | 11 | 116786951 | intron variant | C/T | snv | 8.6E-03 | 1.0E-02 | 1 | |||
| rs3135507 | 0.925 | 0.120 | 11 | 116790772 | missense variant | C/T | snv | 5.0E-02 | 5.5E-02 | 1 |