Source: GWASDB
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12127701 | 1 | 109295642 | intron variant | A/G | snv | 6.2E-02 | 3 | ||||
| rs17645031 | 1 | 109292316 | downstream gene variant | C/T | snv | 7.9E-02 | 3 | ||||
| rs41306199 | 1 | 109292541 | 3 prime UTR variant | C/T | snv | 7.8E-02 | 3 | ||||
| rs413582 | 1 | 109308504 | upstream gene variant | C/T | snv | 0.37 | 3 | ||||
| rs629001 | 1 | 109296296 | missense variant | C/G;T | snv | 0.93 | 3 |