Source: UNIPROT
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs121913355 | 0.641 | 0.520 | 7 | 140781602 | missense variant | C/A;G;T | snv | 4.0E-06 | 4 | ||
| rs121913341 | 0.851 | 0.280 | 7 | 140753350 | missense variant | A/C;T | snv | 2 | |||
| rs121913351 | 0.776 | 0.240 | 7 | 140781611 | missense variant | C/A;G;T | snv | 4.0E-06 | 2 | ||
| rs121913364 | 0.641 | 0.520 | 7 | 140753334 | missense variant | T/C;G | snv | 4.0E-06 | 2 | ||
| rs113488022 | 0.351 | 0.840 | 7 | 140753336 | missense variant | A/C;G;T | snv | 4.0E-06 | 1 | ||
| rs121913338 | 0.677 | 0.400 | 7 | 140753354 | missense variant | T/A;C;G | snv | 1 | |||
| rs121913348 | 0.763 | 0.480 | 7 | 140781617 | missense variant | C/A;G;T | snv | 1 | |||
| rs121913357 | 0.742 | 0.320 | 7 | 140781603 | stop gained | C/A;G;T | snv | 1 | |||
| rs121913361 | 0.807 | 0.280 | 7 | 140753349 | missense variant | C/A;G;T | snv | 1 | |||
| rs121913366 | 0.763 | 0.400 | 7 | 140753345 | missense variant | A/C;T | snv | 1 | |||
| rs121913369 | 0.790 | 0.280 | 7 | 140753346 | missense variant | G/A;C | snv | 4.0E-06 | 1 | ||
| rs121913370 | 0.763 | 0.360 | 7 | 140753393 | missense variant | T/C;G | snv | 1 | |||
| rs121913375 | 0.851 | 0.240 | 7 | 140753339 | missense variant | G/A;C | snv | 1 |