| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1057517954 | 1.000 | 0.160 | X | 153725754 | missense variant | G/A | snv | 1 | |||
| rs1064793877 | 1.000 | 0.160 | X | 153743250 | missense variant | C/T | snv | 1 | |||
| rs11146842 | 1.000 | 0.160 | X | 153743056 | missense variant | G/A | snv | 1 | |||
| rs111966833 | 0.776 | 0.320 | 5 | 147828053 | missense variant | G/A;C | snv | 4.5E-03 | 8 | ||
| rs1131691743 | 1.000 | 0.160 | X | 153726027 | missense variant | C/T | snv | 1 | |||
| rs1131691916 | 1.000 | 0.160 | X | 153725831 | missense variant | C/T | snv | 1 | |||
| rs1131691954 | 1.000 | 0.160 | X | 153726146 | missense variant | G/A | snv | 1 | |||
| rs1170974058 | 1.000 | 0.160 | X | 153743495 | stop gained | C/A;T | snv | 2.8E-05 | 1 | ||
| rs1223231582 | 0.677 | 0.280 | 7 | 142750639 | missense variant | A/G | snv | 7.0E-06 | 24 | ||
| rs128624213 | 1.000 | 0.160 | X | 153726137 | missense variant | G/A | snv | 1 | |||
| rs128624214 | 1.000 | 0.160 | X | 153737214 | missense variant | C/G | snv | 1 | |||
| rs128624215 | 1.000 | 0.160 | X | 153736195 | missense variant | C/G;T | snv | 1 | |||
| rs128624216 | 1.000 | 0.160 | X | 153725709 | missense variant | A/G | snv | 1 | |||
| rs128624217 | 1.000 | 0.160 | X | 153725786 | missense variant | T/G | snv | 1 | |||
| rs128624218 | 1.000 | 0.160 | X | 153726062 | missense variant | G/A | snv | 1 | |||
| rs128624219 | 1.000 | 0.160 | X | 153736232 | missense variant | G/A | snv | 1 | |||
| rs128624220 | 1.000 | 0.160 | X | 153736372 | missense variant | C/T | snv | 1 | |||
| rs128624221 | 1.000 | 0.160 | X | 153736510 | stop gained | C/T | snv | 1 | |||
| rs128624222 | 1.000 | 0.160 | X | 153737192 | stop gained | G/A;T | snv | 2.2E-05 | 1 | ||
| rs128624223 | 0.925 | 0.160 | X | 153740147 | missense variant | C/T | snv | 2 | |||
| rs128624224 | 1.000 | 0.160 | X | 153740155 | missense variant | C/G;T | snv | 1 | |||
| rs128624225 | 0.925 | 0.160 | X | 153743023 | missense variant | C/T | snv | 9.4E-06 | 2 | ||
| rs1411452933 | 1.000 | 0.160 | 7 | 138106690 | missense variant | C/T | snv | 1.2E-05 | 7.0E-06 | 1 | |
| rs150346282 | 1.000 | 0.160 | X | 153743031 | missense variant | G/A | snv | 1 | |||
| rs1557052133 | 1.000 | 0.160 | X | 153725282 | frameshift variant | AGGCCCC/CT | delins | 1 |