| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1060499549 | 0.882 | 0.120 | 9 | 106927699 | stop gained | C/T | snv | 4 | |||
| rs17723637 | 0.882 | 0.080 | 9 | 106925122 | missense variant | A/G | snv | 0.14 | 0.13 | 3 | |
| rs4743034 | 1.000 | 0.080 | 9 | 106870072 | intron variant | G/A | snv | 0.27 | 3 | ||
| rs1060499550 | 1.000 | 0.080 | 9 | 106926891 | frameshift variant | TG/A | delins | 1 | |||
| rs1060499551 | 1.000 | 0.080 | 9 | 106928174 | frameshift variant | A/- | delins | 1 | |||
| rs10978677 | 9 | 106923180 | intron variant | C/A;T | snv | 1 | |||||
| rs35699219 | 9 | 106882096 | intron variant | A/G | snv | 0.18 | 1 | ||||
| rs6477547 | 9 | 106882584 | intron variant | C/T | snv | 0.43 | 1 | ||||
| rs7020564 | 9 | 106907735 | intron variant | A/C;T | snv | 1 | |||||
| rs73667301 | 1.000 | 0.080 | 9 | 106865770 | intron variant | A/G | snv | 7.6E-02 | 1 | ||
| rs7858917 | 9 | 106881599 | intron variant | T/A;C | snv | 1 | |||||
| rs7874161 | 9 | 106876781 | intron variant | C/T | snv | 0.41 | 1 | ||||
| rs10978698 | 9 | 107001923 | intron variant | C/T | snv | 0.23 | 1 | ||||
| rs1876985 | 9 | 106999763 | intron variant | A/C;T | snv | 1 |