| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs483352804 | 0.925 | 0.080 | X | 70035389 | missense variant | G/A;T | snv | 2 | |||
| rs114632254 | 1.000 | 1 | 236482309 | missense variant | C/T | snv | 2.1E-02 | 2.1E-02 | 1 | ||
| rs1292564852 | 1.000 | 4 | 1805414 | missense variant | C/T | snv | 7.0E-06 | 1 | |||
| rs1444216093 | 1.000 | 4 | 5632031 | missense variant | G/A;C | snv | 1 | ||||
| rs17015215 | 1.000 | 1 | 209790735 | missense variant | C/T | snv | 1 | ||||
| rs752627281 | 1.000 | 8 | 38419631 | missense variant | C/T | snv | 2.4E-05 | 6.3E-05 | 1 | ||
| rs758420403 | 1.000 | 4 | 5689210 | missense variant | A/C | snv | 4.0E-06 | 1 | |||
| rs777307167 | 1.000 | 2 | 218890128 | missense variant | T/C | snv | 1.2E-05 | 1 | |||
| rs994158401 | 1.000 | 4 | 4860050 | missense variant | A/G | snv | 1.4E-03 | 1.7E-04 | 1 | ||
| rs12532 | 0.790 | 0.200 | 4 | 4863419 | 3 prime UTR variant | A/G | snv | 0.36 | 10 | ||
| rs3178250 | 0.827 | 0.080 | 20 | 6779554 | 3 prime UTR variant | T/C | snv | 0.21 | 5 | ||
| rs8670 | 0.925 | 0.080 | 4 | 4863149 | 3 prime UTR variant | C/T | snv | 0.22 | 0.23 | 4 | |
| rs1095 | 0.925 | 0.080 | 4 | 4863211 | 3 prime UTR variant | C/T | snv | 1.5E-02 | 2 | ||
| rs15705 | 1.000 | 20 | 6779333 | 3 prime UTR variant | A/C;T | snv | 1 | ||||
| rs7802 | 1.000 | 1 | 209785814 | 3 prime UTR variant | A/G | snv | 7.0E-04 | 1 | |||
| rs861019 | 0.925 | 0.120 | 1 | 209802041 | splice region variant | A/G | snv | 0.44 | 2 | ||
| rs17563 | 0.790 | 0.320 | 14 | 53950804 | stop lost | A/G | snv | 0.45 | 0.44 | 8 | |
| rs2252070 | 0.752 | 0.320 | 11 | 102955810 | upstream gene variant | C/T | snv | 0.68 | 13 | ||
| rs8049367 | 0.851 | 0.240 | 16 | 3930444 | downstream gene variant | T/C | snv | 0.37 | 4 |