| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs7731626 | 0.716 | 0.240 | 5 | 56148856 | intron variant | G/A | snv | 0.30 | 15 | ||
| rs71624119 | 0.776 | 0.200 | 5 | 56144903 | intron variant | G/A | snv | 0.17 | 7 | ||
| rs10213692 | 0.807 | 0.120 | 5 | 56146422 | intron variant | T/C | snv | 0.17 | 6 | ||
| rs28722705 | 5 | 56158115 | intron variant | A/T | snv | 9.9E-02 | 3 | ||||
| rs6859219 | 0.925 | 0.160 | 5 | 56142753 | intron variant | C/A | snv | 0.20 | 2 | ||
| rs10065637 | 1.000 | 0.040 | 5 | 56143024 | intron variant | C/T | snv | 0.15 | 2 | ||
| rs4700060 | 1.000 | 0.080 | 5 | 56214829 | intron variant | C/T | snv | 8.7E-02 | 1 | ||
| rs159547 | 1.000 | 0.040 | 5 | 56163537 | intron variant | T/A;G | snv | 1 | |||
| rs13186299 | 1.000 | 0.040 | 5 | 56159818 | intron variant | G/C;T | snv | 9.7E-02 | 1 | ||
| rs159572 | 1.000 | 0.040 | 5 | 56211219 | intron variant | A/C | snv | 0.37 | 1 |