| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11191454 | 0.776 | 0.160 | 10 | 102900247 | intron variant | A/G | snv | 7.9E-02 | 5 | ||
| rs1046778 | 0.851 | 0.160 | 10 | 102901727 | 3 prime UTR variant | T/C | snv | 0.30 | 3 | ||
| rs4129148 | 1.000 | 0.040 | Y | 1029445 | intergenic variant | C/G;T | snv | 1 | |||
| rs7914558 | 0.851 | 0.040 | 10 | 103016151 | intron variant | G/A | snv | 0.40 | 1 | ||
| rs3787283 | 0.882 | 0.040 | 20 | 10303770 | intron variant | A/G | snv | 0.34 | 3 | ||
| rs3746544 | 0.790 | 0.120 | 20 | 10306436 | 3 prime UTR variant | G/T | snv | 0.68 | 10 | ||
| rs11191580 | 0.827 | 0.040 | 10 | 103146454 | intron variant | T/C | snv | 7.9E-02 | 2 | ||
| rs202213518 | 1.000 | 0.040 | 10 | 103197862 | upstream gene variant | AA/-;A;AAA | delins | 1 | |||
| rs117992169 | 1.000 | 0.040 | 10 | 103425101 | missense variant | G/A | snv | 1.8E-03 | 6.9E-04 | 1 | |
| rs736707 | 0.851 | 0.040 | 7 | 103489956 | intron variant | A/G | snv | 0.30 | 6 | ||
| rs761198705 | 1.000 | 0.040 | 7 | 103490698 | missense variant | G/C | snv | 4.0E-06 | 1 | ||
| rs362746 | 0.925 | 0.120 | 7 | 103539148 | synonymous variant | A/G | snv | 3.8E-02 | 2.1E-02 | 2 | |
| rs362719 | 0.925 | 0.040 | 7 | 103545430 | intron variant | C/A | snv | 0.32 | 2 | ||
| rs362814 | 1.000 | 0.040 | 7 | 103574673 | intron variant | T/A | snv | 0.75 | 1 | ||
| rs540058 | 1.000 | 0.040 | 7 | 103719273 | intron variant | T/C | snv | 0.13 | 1 | ||
| rs661575 | 1.000 | 0.040 | 7 | 103757660 | intron variant | T/A;C | snv | 1 | |||
| rs7341475 | 0.851 | 0.240 | 7 | 103764368 | intron variant | G/A | snv | 0.17 | 5 | ||
| rs475827 | 1.000 | 0.040 | X | 103775144 | intron variant | G/A | snv | 0.20 | 1 | ||
| rs262355 | 1.000 | 0.040 | 7 | 103785668 | intron variant | A/T | snv | 0.67 | 1 | ||
| rs39339 | 1.000 | 0.040 | 7 | 103819488 | intron variant | T/G | snv | 0.17 | 1 | ||
| rs12705169 | 1.000 | 0.040 | 7 | 103936441 | intron variant | T/C;G | snv | 1 | |||
| rs1330075052 | 0.882 | 0.160 | 12 | 104215828 | missense variant | T/C | snv | 1.4E-05 | 3 | ||
| rs779529169 | 1.000 | 0.040 | 12 | 104289006 | frameshift variant | GA/- | delins | 5.6E-05 | 3.5E-05 | 1 | |
| rs1322643228 | 0.807 | 0.280 | 12 | 104321110 | missense variant | C/T | snv | 7.1E-06 | 6 | ||
| rs2498804 | 0.827 | 0.160 | 14 | 104766758 | intron variant | C/A;T | snv | 0.40 | 0.33 | 8 |