| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12755054 | 1.000 | 0.040 | 1 | 196977900 | intron variant | T/A;C | snv | 2 | |||
| rs1750311 | 1.000 | 0.040 | 1 | 196985095 | intron variant | C/A | snv | 0.43 | 2 | ||
| rs1759016 | 1.000 | 0.040 | 1 | 196983368 | intron variant | C/T | snv | 0.43 | 2 | ||
| rs10922153 | 1.000 | 0.040 | 1 | 197009485 | 3 prime UTR variant | T/G | snv | 0.38 | 1 | ||
| rs10922152 | 1.000 | 0.040 | 1 | 196993876 | intron variant | T/A | snv | 0.38 | 1 | ||
| rs10801582 | 1 | 196975227 | upstream gene variant | G/A | snv | 0.22 | 1 | ||||
| rs12116643 | 1 | 197004053 | intron variant | T/C | snv | 0.19 | 1 |