Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1569292214 | 1.000 | 0.120 | X | 101358408 | missense variant | A/T | snv | 4 | |||
| rs128620183 | 0.925 | 0.120 | X | 101354687 | missense variant | C/T | snv | 2 | |||
| rs128621193 | 0.925 | 0.120 | X | 101360581 | stop gained | G/A | snv | 2 | |||
| rs128621195 | 1.000 | 0.120 | X | 101358672 | missense variant | T/C | snv | 2 | |||
| rs1555980049 | 0.925 | 0.120 | X | 101370018 | stop gained | C/T | snv | 2 | |||
| rs104894770 | 1.000 | 0.120 | X | 101353935 | missense variant | C/G | snv | 1 | |||
| rs1131691354 | 1.000 | 0.120 | X | 101386057 | splice region variant | C/A;T | snv | 1 | |||
| rs128620184 | 1.000 | 0.120 | X | 101356845 | missense variant | T/C | snv | 1 | |||
| rs128620186 | 1.000 | 0.120 | X | 101375283 | start lost | A/G | snv | 1 | |||
| rs128620187 | 1.000 | 0.120 | X | 101375248 | stop gained | G/A | snv | 1 | |||
| rs128620188 | 1.000 | 0.120 | X | 101375242 | stop gained | G/A | snv | 1 | |||
| rs128620189 | 1.000 | 0.120 | X | 101375188 | missense variant | T/G | snv | 1 | |||
| rs128621190 | 1.000 | 0.120 | X | 101370051 | missense variant | A/T | snv | 1 | |||
| rs128621191 | 1.000 | 0.120 | X | 101360626 | stop gained | C/A | snv | 1 | |||
| rs128621192 | 1.000 | 0.120 | X | 101360589 | stop gained | C/T | snv | 1 | |||
| rs128621196 | 1.000 | 0.120 | X | 101358411 | missense variant | T/G | snv | 1 | |||
| rs128621198 | 1.000 | 0.120 | X | 101356910 | missense variant | A/G | snv | 1 | |||
| rs128621199 | 1.000 | 0.120 | X | 101356858 | stop gained | G/A;T | snv | 1.1E-05 | 1 | ||
| rs128621200 | 1.000 | 0.120 | X | 101356102 | missense variant | A/G | snv | 1 | |||
| rs128621205 | 1.000 | 0.120 | X | 101353879 | missense variant | A/G | snv | 1 | |||
| rs128621206 | 1.000 | 0.120 | X | 101353336 | missense variant | T/C | snv | 1 | |||
| rs128621207 | 1.000 | 0.120 | X | 101353329 | stop gained | G/T | snv | 1 | |||
| rs128621208 | 1.000 | 0.120 | X | 101353282 | missense variant | G/T | snv | 1 | |||
| rs128621209 | 1.000 | 0.120 | X | 101353264 | missense variant | C/T | snv | 1 | |||
| rs128621210 | 1.000 | 0.120 | X | 101353213 | missense variant | A/T | snv | 1 |