| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs79246196 | 0.925 | 0.080 | 7 | 100185286 | intron variant | C/T | snv | 1.8E-02 | 4 | ||
| rs1427074798 | 1.000 | 0.080 | 10 | 100297067 | synonymous variant | A/G | snv | 4.0E-06 | 1 | ||
| rs57083693 | 1.000 | 0.080 | 12 | 101348402 | intron variant | T/C | snv | 0.23 | 3 | ||
| rs12544026 | 0.925 | 0.080 | 8 | 101819970 | intron variant | G/A | snv | 0.85 | 4 | ||
| rs3917328 | 1.000 | 0.080 | 2 | 102178081 | 3 prime UTR variant | C/G;T | snv | 5.1E-02 | 2 | ||
| rs13107325 | 0.776 | 0.520 | 4 | 102267552 | missense variant | C/A;T | snv | 4.0E-06; 4.5E-02 | 34 | ||
| rs774062108 | 0.925 | 0.240 | 4 | 102607651 | splice region variant | T/G | snv | 4.0E-06 | 3 | ||
| rs4648143 | 1.000 | 0.080 | 4 | 102616617 | 3 prime UTR variant | G/A;T | snv | 5.0E-03; 4.0E-06 | 2 | ||
| rs115357105 | 0.925 | 0.080 | 9 | 104376689 | intergenic variant | A/G | snv | 1.5E-02 | 4 | ||
| rs61776290 | 1.000 | 0.080 | 1 | 10634850 | upstream gene variant | C/T | snv | 8.7E-02 | 3 | ||
| rs17037102 | 0.807 | 0.240 | 4 | 106924637 | missense variant | C/A;T | snv | 0.15 | 6 | ||
| rs7906104 | 1.000 | 0.080 | 10 | 108737343 | intron variant | C/T | snv | 0.29 | 3 | ||
| rs1995364 | 1.000 | 0.080 | 5 | 10903669 | intergenic variant | A/G | snv | 0.62 | 1 | ||
| rs17125651 | 1.000 | 0.080 | 10 | 109063325 | intergenic variant | T/C | snv | 0.14 | 3 | ||
| rs521674 | 0.925 | 0.160 | 10 | 111075832 | upstream gene variant | T/A | snv | 0.57 | 2 | ||
| rs602618 | 1.000 | 0.080 | 10 | 111083327 | downstream gene variant | C/A | snv | 0.58 | 1 | ||
| rs149212747 | 1.000 | 0.080 | 12 | 111398968 | intron variant | C/-;CC;CCC | delins | 2 | |||
| rs25917 | 1.000 | 0.080 | 5 | 111473151 | intron variant | A/G | snv | 0.11 | 1 | ||
| rs3782886 | 0.724 | 0.480 | 12 | 111672685 | synonymous variant | T/C | snv | 1.9E-02 | 5.9E-03 | 22 | |
| rs11066001 | 0.763 | 0.360 | 12 | 111681367 | intron variant | T/C | snv | 5.8E-03 | 15 | ||
| rs886205 | 0.827 | 0.360 | 12 | 111766623 | intron variant | A/G | snv | 0.35 | 8 | ||
| rs201745983 | 0.752 | 0.200 | 12 | 111783219 | missense variant | G/A | snv | 6.8E-05 | 7.7E-05 | 14 | |
| rs940553638 | 0.827 | 0.200 | 12 | 111783222 | missense variant | G/A | snv | 1.6E-05 | 7.0E-06 | 6 | |
| rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 116 | |
| rs143894582 | 1.000 | 0.080 | 12 | 112469070 | intron variant | A/-;AA | delins | 3 |