| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs16139 | 0.658 | 0.560 | 7 | 24285260 | missense variant | T/A;C | snv | 4.0E-06; 3.0E-02 | 36 | ||
| rs16147 | 0.695 | 0.400 | 7 | 24283791 | upstream gene variant | T/C | snv | 0.48 | 18 | ||
| rs5574 | 0.882 | 0.200 | 7 | 24289514 | synonymous variant | C/T | snv | 0.43 | 0.43 | 5 | |
| rs1356639869 | 1.000 | 0.040 | 7 | 24289527 | missense variant | C/A | snv | 2 | |||
| rs17149106 | 0.925 | 0.160 | 7 | 24283588 | upstream gene variant | G/T | snv | 2 | |||
| rs1468271 | 1.000 | 0.040 | 7 | 24287362 | intron variant | C/T | snv | 0.97 | 2 | ||
| rs16128 | 0.925 | 0.080 | 7 | 24291425 | intron variant | C/A | snv | 2 | |||
| rs16475 | 0.925 | 0.120 | 7 | 24291867 | downstream gene variant | A/G | snv | 5.3E-02 | 2 | ||
| rs16131 | 1.000 | 0.080 | 7 | 24290218 | intron variant | T/A;C | snv | 1 | |||
| rs16148 | 7 | 24282719 | upstream gene variant | T/C | snv | 0.42 | 1 | ||||
| rs778902328 | 1.000 | 0.040 | 7 | 24291679 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 1 | |
| rs16476 | 7 | 24290600 | intron variant | T/G | snv | 0.44 | 1 |