Source: ALL
| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs734312 | 0.790 | 0.240 | 4 | 6301627 | missense variant | G/A | snv | 0.55 | 0.42 | 10 | |
| rs10010131 | 0.827 | 0.120 | 4 | 6291188 | intron variant | A/G | snv | 0.66 | 0.63 | 7 | |
| rs4689388 | 0.882 | 0.360 | 4 | 6268329 | upstream gene variant | G/A | snv | 0.64 | 4 | ||
| rs4458523 | 1.000 | 0.080 | 4 | 6288259 | intron variant | T/G | snv | 0.61 | 3 | ||
| rs752854 | 0.925 | 0.080 | 4 | 6280234 | intron variant | C/G;T | snv | 3 | |||
| rs10012946 | 1.000 | 0.080 | 4 | 6291623 | intron variant | T/C | snv | 0.63 | 1 | ||
| rs1553876668 | 1.000 | 0.080 | 4 | 6289001 | stop gained | C/A | snv | 1 | |||
| rs1801212 | 1.000 | 0.080 | 4 | 6300792 | missense variant | G/A;C;T | snv | 0.78 | 1 | ||
| rs1801214 | 1.000 | 0.080 | 4 | 6301295 | missense variant | C/A;G;T | snv | 0.67 | 1 | ||
| rs3821943 | 1.000 | 0.080 | 4 | 6298213 | intron variant | C/T | snv | 0.50 | 1 | ||
| rs4320200 | 1.000 | 0.080 | 4 | 6269316 | upstream gene variant | A/T | snv | 0.56 | 1 | ||
| rs4416547 | 1.000 | 0.080 | 4 | 6292240 | intron variant | G/A | snv | 0.63 | 1 | ||
| rs4688985 | 1.000 | 0.080 | 4 | 6283988 | intron variant | A/G | snv | 0.79 | 1 | ||
| rs6446482 | 1.000 | 0.080 | 4 | 6293966 | intron variant | C/G | snv | 0.63 | 1 |