| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs6651252 | 0.790 | 0.200 | 8 | 128554935 | intron variant | T/C | snv | 0.19 | 8 | ||
| rs11785816 | 0.882 | 8 | 128518940 | intron variant | C/A;G | snv | 4 | ||||
| rs1561927 | 0.807 | 0.280 | 8 | 128555832 | intron variant | C/T | snv | 0.65 | 2 | ||
| rs10088218 | 0.851 | 0.120 | 8 | 128531703 | intron variant | G/A | snv | 0.13 | 2 | ||
| rs1400482 | 0.925 | 0.120 | 8 | 128529685 | intron variant | G/A | snv | 0.13 | 2 | ||
| rs1516971 | 1.000 | 0.120 | 8 | 128529854 | intron variant | T/C | snv | 0.19 | 1 | ||
| rs7815944 | 1.000 | 0.120 | 8 | 128415272 | intron variant | A/G | snv | 0.12 | 1 | ||
| rs1561924 | 1.000 | 0.040 | 8 | 128557125 | intron variant | G/A | snv | 0.18 | 1 | ||
| rs67824503 | 1.000 | 0.040 | 8 | 128523018 | intron variant | T/C | snv | 0.23 | 1 | ||
| rs17232730 | 1.000 | 0.080 | 8 | 128525500 | intron variant | G/C | snv | 9.8E-02 | 1 | ||
| rs35286446 | 1.000 | 0.080 | 8 | 128433618 | intron variant | TATATA/-;TATA;TATATATA;TATATATATA | delins | 1 | |||
| rs4598218 | 8 | 128471710 | intron variant | C/T | snv | 0.48 | 1 | ||||
| rs17804358 | 8 | 128439451 | intron variant | C/T | snv | 0.48 | 1 |