| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs11554137 | 0.742 | 0.040 | 2 | 208248468 | synonymous variant | G/A | snv | 5.1E-02 | 6.8E-02 | 13 | |
| rs1482518887 | 0.790 | 0.040 | 21 | 34887018 | missense variant | C/T | snv | 7.0E-06 | 8 | ||
| rs138817062 | 0.882 | 0.040 | 15 | 74044940 | missense variant | C/T | snv | 4.0E-05 | 7.0E-06 | 4 | |
| rs35602083 | 0.851 | 0.040 | 13 | 28049450 | missense variant | C/T | snv | 1.7E-02 | 1.6E-02 | 4 | |
| rs212090 | 1.000 | 0.040 | 16 | 16142147 | 3 prime UTR variant | T/A | snv | 0.36 | 3 | ||
| rs3213409 | 0.925 | 0.040 | 19 | 17834887 | missense variant | C/T | snv | 8.6E-03 | 7.3E-03 | 3 | |
| rs3842803 | 0.925 | 0.040 | 9 | 122392256 | synonymous variant | T/C | snv | 2.4E-02 | 8.2E-02 | 3 | |
| rs713330 | 1.000 | 0.040 | 11 | 35202398 | intron variant | C/T | snv | 0.74 | 3 | ||
| rs767580335 | 1.000 | 0.040 | 3 | 12590826 | missense variant | T/C;G | snv | 2.4E-05; 4.0E-06 | 3 | ||
| rs7729269 | 0.925 | 0.040 | 5 | 113384697 | intron variant | T/C | snv | 0.17 | 3 | ||
| rs1057520026 | 0.925 | 0.040 | 13 | 28028244 | missense variant | T/G | snv | 2 | |||
| rs1178981336 | 1.000 | 0.040 | 9 | 113424228 | frameshift variant | -/G | delins | 7.0E-06 | 2 | ||
| rs142883642 | 1.000 | 0.040 | 2 | 208248486 | missense variant | T/C | snv | 3.6E-05 | 2.1E-05 | 2 | |
| rs1801020 | 1.000 | 0.040 | 5 | 177409531 | 5 prime UTR variant | A/G | snv | 0.65 | 0.67 | 2 | |
| rs183484 | 0.925 | 0.040 | 11 | 4119902 | synonymous variant | C/A | snv | 0.45 | 0.39 | 2 | |
| rs2268276 | 0.925 | 0.040 | 21 | 34808717 | intron variant | G/A | snv | 0.38 | 2 | ||
| rs2304205 | 0.925 | 0.040 | 19 | 49665670 | splice donor variant | A/C;T | snv | 0.36 | 2 | ||
| rs233112 | 0.925 | 0.040 | 1 | 85320068 | 3 prime UTR variant | T/C | snv | 0.37 | 2 | ||
| rs2393726 | 0.925 | 0.040 | 10 | 62094648 | 3 prime UTR variant | A/G | snv | 3.9E-02 | 2 | ||
| rs2897047 | 0.925 | 0.040 | 5 | 2640009 | regulatory region variant | A/G | snv | 0.63 | 2 | ||
| rs3212723 | 0.925 | 0.040 | 19 | 17843406 | missense variant | G/T | snv | 6.2E-03 | 2.6E-02 | 2 | |
| rs3744660 | 0.925 | 0.040 | 17 | 51168540 | intron variant | G/A | snv | 0.16 | 2 | ||
| rs4643786 | 0.925 | 0.040 | 4 | 71029543 | 3 prime UTR variant | C/G;T | snv | 2 | |||
| rs6415872 | 0.925 | 0.040 | 10 | 61900930 | upstream gene variant | G/A | snv | 0.51 | 2 | ||
| rs767232094 | 1.000 | 0.040 | 16 | 55484157 | synonymous variant | C/T | snv | 8.0E-06 | 2 |