| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs56378716 | 1.000 | 0.080 | 17 | 58279141 | missense variant | A/G | snv | 1.0E-02 | 9.8E-03 | 6 | |
| rs35897051 | 1.000 | 0.080 | 17 | 58270865 | splice acceptor variant | T/G | snv | 4.4E-03 | 4.6E-03 | 3 | |
| rs28730837 | 1.000 | 0.080 | 17 | 58278036 | missense variant | G/A | snv | 1.2E-02 | 1.2E-02 | 2 | |
| rs119468010 | 1.000 | 0.080 | 17 | 58272835 | missense variant | G/A | snv | 1.5E-03 | 1.7E-03 | 1 | |
| rs119469012 | 1.000 | 0.080 | 17 | 58272825 | missense variant | A/C;G | snv | 1 | |||
| rs119469013 | 1.000 | 0.080 | 17 | 58273534 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
| rs119469014 | 1.000 | 0.080 | 17 | 58273540 | missense variant | G/A;C | snv | 2.4E-05; 2.0E-05 | 1 | ||
| rs536522394 | 1.000 | 0.080 | 17 | 58273467 | frameshift variant | TTGGGTTCCATGGG/-;TTGGGTTCCATGGGTTGGGTTCCATGGG | delins | 8.3E-04 | 1 | ||
| rs78950939 | 1.000 | 0.080 | 17 | 58279553 | missense variant | T/C | snv | 4.6E-04 | 5.0E-04 | 1 |