| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4657412 | 1.000 | 1 | 165207796 | intron variant | G/A | snv | 0.79 | 1 | |||
| rs57302492 | 1.000 | 2 | 70831099 | missense variant | T/A | snv | 7.0E-02 | 8.9E-02 | 1 | ||
| rs749569169 | 1.000 | 7 | 29512676 | missense variant | A/G | snv | 4.0E-06 | 1 | |||
| rs756151230 | 1.000 | 7 | 92470377 | missense variant | G/C | snv | 1 | ||||
| rs774027752 | 1.000 | 19 | 40845472 | missense variant | T/C | snv | 8.0E-06 | 1.4E-05 | 1 | ||
| rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 |