| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs12777 | 5 | 132335969 | synonymous variant | C/G | snv | 3.1E-02 | 2.8E-02 | 3 | |||
| rs270607 | 5 | 132313493 | intron variant | A/G | snv | 0.69 | 3 | ||||
| rs272889 | 5 | 132329685 | intron variant | A/G | snv | 0.64 | 2 | ||||
| rs274546 | 5 | 132364175 | intron variant | A/G;T | snv | 1 | |||||
| rs10058074 | 5 | 132350453 | intron variant | G/A | snv | 0.31 | 1 | ||||
| rs272888 | 1.000 | 0.040 | 5 | 132329730 | intron variant | T/C | snv | 0.71 | 1 | ||
| rs1050152 | 0.776 | 0.480 | 5 | 132340627 | missense variant | C/T | snv | 0.29 | 0.28 | 1 | |
| rs273909 | 1.000 | 0.040 | 5 | 132331660 | intron variant | A/G | snv | 9.5E-02 | 1 |