| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs10230087 | 1.000 | 0.040 | 7 | 114614352 | intron variant | G/A | snv | 0.73 | 2 | ||
| rs1163276899 | 1.000 | 0.040 | 3 | 53673125 | missense variant | G/A | snv | 2 | |||
| rs12037377 | 1.000 | 0.040 | 1 | 246551218 | missense variant | G/A | snv | 3.2E-03 | 1.6E-03 | 2 | |
| rs12531289 | 1.000 | 0.040 | 7 | 114600061 | intron variant | T/A | snv | 0.73 | 2 | ||
| rs1275980031 | 1.000 | 0.040 | 7 | 103540259 | missense variant | G/A | snv | 4.0E-06 | 2 | ||
| rs1350135 | 1.000 | 0.040 | 7 | 114602621 | intron variant | C/A;G;T | snv | 2 | |||
| rs1801291 | 1.000 | 0.040 | X | 43744144 | synonymous variant | T/C | snv | 2 | |||
| rs1804197 | 1.000 | 0.040 | 5 | 112844212 | 3 prime UTR variant | C/A | snv | 7.2E-02 | 2 | ||
| rs199473391 | 1.000 | 0.040 | 12 | 2607117 | stop gained | G/A;T | snv | 2 | |||
| rs2061183 | 1.000 | 0.040 | 7 | 114617959 | intron variant | C/G | snv | 0.73 | 2 | ||
| rs251684 | 1.000 | 0.040 | 19 | 48098197 | synonymous variant | T/C | snv | 0.61 | 0.64 | 2 | |
| rs4541 | 1.000 | 0.040 | 8 | 142875277 | missense variant | G/A;T | snv | 7.8E-02; 2.0E-05 | 2 | ||
| rs9616915 | 1.000 | 0.040 | 22 | 50679152 | missense variant | T/C | snv | 0.43 | 0.46 | 2 | |
| rs201551401 | 0.925 | 0.040 | 7 | 124746694 | missense variant | C/T | snv | 6.4E-05 | 1.4E-05 | 3 | |
| rs237902 | 0.925 | 0.040 | 3 | 8767498 | synonymous variant | G/A | snv | 0.29 | 0.31 | 3 | |
| rs3027407 | 0.925 | 0.040 | X | 43745594 | 3 prime UTR variant | A/G | snv | 3 | |||
| rs3747333 | 0.925 | 0.040 | X | 5893491 | missense variant | G/A;C;T | snv | 7.6E-03 | 3 | ||
| rs3747334 | 0.925 | 0.040 | X | 5893489 | synonymous variant | G/A;C;T | snv | 1.2E-05; 6.7E-03 | 3 | ||
| rs4141463 | 0.925 | 0.040 | 20 | 14766825 | intron variant | T/C | snv | 0.50 | 3 | ||
| rs4534 | 0.925 | 0.240 | 8 | 142879686 | missense variant | C/T | snv | 8.4E-02 | 4.1E-02 | 3 | |
| rs587777457 | 0.925 | 0.200 | X | 43731695 | missense variant | G/T | snv | 3 | |||
| rs750257282 | 1.000 | 0.040 | 11 | 3038127 | missense variant | C/G;T | snv | 3.2E-05 | 3 | ||
| rs768913131 | 0.925 | 0.040 | 2 | 50552821 | missense variant | G/A | snv | 3 | |||
| rs1858830 | 0.925 | 0.040 | 7 | 116672385 | 5 prime UTR variant | C/G | snv | 0.40 | 4 | ||
| rs6551665 | 0.882 | 0.040 | 4 | 61873823 | intron variant | G/A | snv | 0.59 | 4 |