| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs2814778 | 0.763 | 0.360 | 1 | 159204893 | 5 prime UTR variant | T/C | snv | 0.25 | 11 | ||
| rs445 | 7 | 92779056 | intron variant | C/T | snv | 0.14 | 9 | ||||
| rs12266014 | 10 | 24922362 | intron variant | C/T | snv | 0.26 | 7 | ||||
| rs143034248 | 11 | 118210555 | missense variant | C/T | snv | 4.0E-03 | 3.5E-03 | 7 | |||
| rs2038700 | 14 | 24992783 | intron variant | T/C | snv | 0.53 | 7 | ||||
| rs34599082 | 1 | 159205704 | missense variant | C/T | snv | 1.1E-02 | 9.9E-03 | 7 | |||
| rs6782228 | 3 | 128604581 | intergenic variant | G/C | snv | 0.28 | 7 | ||||
| rs9260620 | 6 | 29955314 | upstream gene variant | T/G | snv | 0.24 | 7 |