| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs26907 | 0.882 | 0.240 | 5 | 81069496 | intron variant | G/A;T | snv | 3 | |||
| rs973742 | 0.925 | 0.160 | 1 | 158190738 | downstream gene variant | G/A | snv | 0.42 | 2 | ||
| rs128624223 | 0.925 | 0.160 | X | 153740147 | missense variant | C/T | snv | 2 | |||
| rs128624225 | 0.925 | 0.160 | X | 153743023 | missense variant | C/T | snv | 9.4E-06 | 2 | ||
| rs864309520 | 1.000 | 0.160 | X | 153725917 | missense variant | G/C | snv | 2 | |||
| rs781703310 | 1.000 | 0.160 | 7 | 20742967 | missense variant | A/C;G | snv | 4.0E-06; 4.0E-06 | 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 | |||
| rs1170974058 | 1.000 | 0.160 | X | 153743495 | stop gained | C/A;T | snv | 2.8E-05 | 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 | |||
| 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 | ||
| rs128624224 | 1.000 | 0.160 | X | 153740155 | missense variant | C/G;T | snv | 1 | |||
| rs150346282 | 1.000 | 0.160 | X | 153743031 | missense variant | G/A | snv | 1 | |||
| rs1557054210 | 1.000 | 0.160 | X | 153736390 | stop gained | C/T | snv | 1 | |||
| rs1557054745 | 1.000 | 0.160 | X | 153740135 | missense variant | G/A | snv | 1 | |||
| rs1557054776 | 1.000 | 0.160 | X | 153740231 | missense variant | C/T | snv | 1 | |||
| rs1557054873 | 1.000 | 0.160 | X | 153740711 | missense variant | G/A | snv | 1 | |||
| rs1557054875 | 1.000 | 0.160 | X | 153740721 | splice donor variant | T/G | snv | 1 | |||
| rs1557055253 | 1.000 | 0.160 | X | 153743024 | frameshift variant | GTGG/- | delins | 1 | |||
| rs1557055260 | 1.000 | 0.160 | X | 153743032 | missense variant | A/G | snv | 1 | |||
| rs1557055316 | 1.000 | 0.160 | X | 153743231 | missense variant | G/A | snv | 1 |