| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 7 | ||
| rs121913273 | 0.605 | 0.440 | 3 | 179218294 | missense variant | G/A;C | snv | 5 | |||
| rs104886003 | 0.562 | 0.440 | 3 | 179218303 | missense variant | G/A;C | snv | 4.0E-06 | 4 | ||
| rs121913272 | 0.752 | 0.400 | 3 | 179210192 | missense variant | T/C;G | snv | 3 | |||
| rs121913274 | 0.645 | 0.320 | 3 | 179218304 | missense variant | A/C;G;T | snv | 3 | |||
| rs121913286 | 0.677 | 0.280 | 3 | 179218306 | missense variant | C/A;G | snv | 2 | |||
| rs121913283 | 0.724 | 0.440 | 3 | 179234286 | missense variant | G/A;T | snv | 4.0E-06 | 2 | ||
| rs397517201 | 0.732 | 0.240 | 3 | 179218307 | missense variant | A/C;G;T | snv | 1 | |||
| rs1057519927 | 0.716 | 0.240 | 3 | 179218295 | missense variant | A/C;G;T | snv | 1 | |||
| rs1057519925 | 0.683 | 0.560 | 3 | 179210291 | missense variant | G/A;C | snv | 1 | |||
| rs772110575 | 0.807 | 0.160 | 3 | 179198938 | missense variant | G/A;T | snv | 4.0E-06 | 1 | ||
| rs1057519930 | 1.000 | 0.080 | 3 | 179199142 | missense variant | G/T | snv | 1 | |||
| rs397517202 | 0.851 | 0.320 | 3 | 179234230 | missense variant | A/G | snv | 1 | |||
| rs121913281 | 0.623 | 0.520 | 3 | 179234296 | missense variant | C/T | snv | 1 | |||
| rs1064793732 | 0.882 | 0.320 | 3 | 179204536 | missense variant | G/A | snv | 1 | |||
| rs121913287 | 0.752 | 0.400 | 3 | 179199088 | missense variant | G/A | snv | 1 | |||
| rs1242945375 | 1.000 | 0.200 | 3 | 179234261 | missense variant | C/T | snv | 1 | |||
| rs867262025 | 0.790 | 0.360 | 3 | 179221146 | missense variant | G/A | snv | 1 | |||
| rs863225460 | 0.882 | 0.200 | 3 | 179199160 | missense variant | T/A | snv | 1 | |||
| rs397514565 | 0.882 | 0.240 | 3 | 179204576 | missense variant | G/A | snv | 1 | |||
| rs587776932 | 0.925 | 0.280 | 3 | 179230077 | missense variant | G/A | snv | 1 | |||
| rs121913288 | 1.000 | 0.200 | 3 | 179234219 | missense variant | A/G | snv | 1 | |||
| rs1057519929 | 0.776 | 0.320 | 3 | 179199066 | missense variant | G/A | snv | 1 | |||
| rs121913277 | 0.925 | 0.280 | 3 | 179234302 | missense variant | G/A;C | snv | 1 | |||
| rs587777794 | 1.000 | 3 | 179204588 | missense variant | G/A | snv | 7.0E-06 | 1 |