Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1718119 | 0.689 | 0.520 | 12 | 121177300 | missense variant | G/A;T | snv | 0.35; 4.0E-06 | 21 | ||
| rs7958311 | 0.851 | 0.160 | 12 | 121167552 | missense variant | G/A;C | snv | 0.25; 4.0E-06 | 5 | ||
| rs2393799 | 0.882 | 0.200 | 12 | 121132209 | upstream gene variant | C/A;T | snv | 3 | |||
| rs208290 | 1.000 | 0.080 | 12 | 121156253 | intron variant | G/A | snv | 0.43 | 1 | ||
| rs656612 | 1.000 | 0.080 | 12 | 121138849 | intron variant | C/A | snv | 0.60 | 1 |