| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs746800707 | 0.851 | 0.160 | 20 | 36240388 | missense variant | G/A;C;T | snv | 1.2E-05; 4.0E-06 | 8 | ||
| rs17436024 | 20 | 36255171 | intron variant | C/T | snv | 2.7E-02 | 2 | ||||
| rs2425204 | 20 | 36268740 | intron variant | A/G | snv | 0.15 | 2 | ||||
| rs12481546 | 20 | 36261760 | intron variant | G/A | snv | 6.9E-03 | 1 | ||||
| rs2425192 | 20 | 36242663 | intron variant | A/G;T | snv | 1 |