Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs137853236 | 0.807 | 0.280 | 12 | 120997504 | missense variant | C/T | snv | 1.2E-05 | 6 | ||
| rs1555212014 | 0.807 | 0.280 | 12 | 120994264 | missense variant | C/T | snv | 6 | |||
| rs754729248 | 0.807 | 0.280 | 12 | 120996568 | missense variant | C/A;G;T | snv | 2.4E-05; 1.9E-04; 3.6E-05 | 6 | ||
| rs137853247 | 0.851 | 0.200 | 12 | 120978860 | missense variant | G/A;C | snv | 7.7E-04; 4.0E-06 | 5 | ||
| rs587776825 | 0.827 | 0.280 | 12 | 120994315 | frameshift variant | C/-;CC;CCC | delins | 5 |