| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11161721 | 1 | 86022231 | intron variant | C/A | snv | 0.27 | 0.27 | 4 | |||
| rs10505232 | 0.925 | 0.040 | 8 | 114878275 | intergenic variant | A/C | snv | 0.11 | 3 | ||
| rs3181382 | 0.925 | 0.040 | 14 | 24320104 | intron variant | G/C;T | snv | 3 | |||
| rs9927732 | 0.925 | 0.040 | 16 | 88043118 | intron variant | C/A;G;T | snv | 3 | |||
| rs372271081 | 1.000 | 0.080 | 1 | 19647903 | intron variant | G/A | snv | 8.4E-02 | 2 | ||
| rs201386833 | X | 116033029 | intergenic variant | T/-;TT | delins | 1 | |||||
| rs2963463 | 5 | 158468041 | downstream gene variant | T/A;C | snv | 1 | |||||
| rs7217780 | 17 | 15287707 | intron variant | C/T | snv | 0.58 | 1 | ||||
| rs201450565 | 3 | 128339767 | intron variant | -/T | delins | 1.7E-04 | 1 | ||||
| rs11466328 | 19 | 41345137 | intron variant | G/A | snv | 2.0E-02 | 1 |