| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913277 | 0.925 | 0.280 | 3 | 179234302 | missense variant | G/A;C | snv | 4 | |||
| rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 101 | ||
| rs121913281 | 0.623 | 0.520 | 3 | 179234296 | missense variant | C/T | snv | 37 | |||
| rs121913282 | 0.882 | 0.040 | 3 | 179221072 | missense variant | A/C | snv | 4 | |||
| rs121913283 | 0.724 | 0.440 | 3 | 179234286 | missense variant | G/A;T | snv | 4.0E-06 | 16 | ||
| rs121913284 | 0.776 | 0.160 | 3 | 179203765 | missense variant | T/A;G | snv | 11 | |||
| rs121913285 | 3 | 179218286 | missense variant | C/G | snv | 1 | |||||
| rs121913286 | 0.677 | 0.280 | 3 | 179218306 | missense variant | C/A;G | snv | 23 | |||
| rs121913287 | 0.752 | 0.400 | 3 | 179199088 | missense variant | G/A | snv | 12 | |||
| rs121913288 | 1.000 | 0.200 | 3 | 179234219 | missense variant | A/G | snv | 2 | |||
| rs1242945375 | 1.000 | 0.200 | 3 | 179234261 | missense variant | C/T | snv | 1 | |||
| rs12494623 | 1.000 | 0.080 | 3 | 179214763 | intron variant | C/G;T | snv | 1 | |||
| rs1260908401 | 1.000 | 3 | 179203565 | missense variant | C/T | snv | 4.0E-06 | 1 | |||
| rs141178472 | 0.925 | 0.080 | 3 | 179234393 | 3 prime UTR variant | T/C | snv | 3.0E-03 | 3.3E-03 | 2 | |
| rs1442481831 | 0.925 | 0.080 | 3 | 179203635 | missense variant | T/C | snv | 2 | |||
| rs1517586 | 3 | 179166120 | intron variant | T/C | snv | 7.1E-02 | 1 | ||||
| rs1553826166 | 1.000 | 0.080 | 3 | 179234231 | missense variant | C/G | snv | 1 | |||
| rs1560137208 | 1.000 | 0.120 | 3 | 179199073 | missense variant | T/C | snv | 1 | |||
| rs1560137609 | 0.925 | 0.080 | 3 | 179199743 | frameshift variant | -/T | delins | 2 | |||
| rs1607237 | 1.000 | 0.040 | 3 | 179232509 | intron variant | C/T | snv | 0.68 | 1 | ||
| rs17849071 | 0.776 | 0.160 | 3 | 179218439 | intron variant | T/G | snv | 7.9E-02 | 8 | ||
| rs17849079 | 0.882 | 0.120 | 3 | 179234232 | synonymous variant | C/T | snv | 2.1E-02 | 1.5E-02 | 3 | |
| rs2677764 | 0.925 | 0.080 | 3 | 179206019 | intron variant | C/A;T | snv | 2 | |||
| rs2699887 | 0.763 | 0.280 | 3 | 179148620 | intron variant | C/T | snv | 0.18 | 11 | ||
| rs2699905 | 3 | 179166549 | intron variant | C/T | snv | 0.19 | 1 |