| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs3735684 | 0.851 | 0.120 | 7 | 985219 | missense variant | G/A | snv | 6.8E-02 | 7.3E-02 | 4 | |
| rs2732875 | 0.790 | 0.080 | X | 9795858 | intron variant | C/G;T | snv | 9 | |||
| rs1801265 | 0.763 | 0.280 | 1 | 97883329 | missense variant | A/G | snv | 0.28 | 13 | ||
| rs5934683 | 0.790 | 0.080 | X | 9783434 | intron variant | T/C | snv | 0.50 | 9 | ||
| rs7988900 | 1.000 | 0.080 | 13 | 97826281 | intergenic variant | T/C | snv | 0.45 | 1 | ||
| rs768288280 | 1.000 | 0.080 | 1 | 97740403 | missense variant | T/C | snv | 4.0E-06 | 2 | ||
| rs150385342 | 1.000 | 0.080 | 1 | 97740400 | missense variant | C/A;T | snv | 4.0E-06 | 1 | ||
| rs10817938 | 0.882 | 0.080 | 9 | 97700127 | non coding transcript exon variant | T/C | snv | 3.2E-02 | 5 | ||
| rs2297595 | 0.776 | 0.320 | 1 | 97699535 | missense variant | T/C | snv | 8.5E-02 | 8.1E-02 | 10 | |
| rs376040996 | 0.790 | 0.120 | 9 | 97687210 | missense variant | T/C;G | snv | 1.2E-05; 2.0E-05 | 7 | ||
| rs1245554802 | 0.851 | 0.120 | 3 | 9765892 | splice acceptor variant | T/C | snv | 4.0E-06 | 5 | ||
| rs11692435 | 0.790 | 0.080 | 2 | 97658891 | missense variant | G/A | snv | 7.0E-02 | 6.7E-02 | 10 | |
| rs771306418 | 0.851 | 0.120 | 3 | 9765885 | splice acceptor variant | -/C | delins | 5 | |||
| rs1052133 | 0.476 | 0.800 | 3 | 9757089 | missense variant | C/G | snv | 0.27 | 0.22 | 147 | |
| rs756363791 | 0.882 | 0.080 | 3 | 9756823 | missense variant | G/A | snv | 2.0E-05 | 4 | ||
| rs113561019 | 1.000 | 0.080 | 3 | 9756791 | missense variant | G/A;T | snv | 3.9E-03; 4.0E-06 | 2 | ||
| rs746702110 | 0.627 | 0.480 | 3 | 9756778 | missense variant | C/T | snv | 1.2E-05 | 2.8E-05 | 38 | |
| rs1400826115 | 1.000 | 0.080 | 3 | 9756770 | missense variant | A/G | snv | 4.0E-06 | 2 | ||
| rs1419684880 | 1.000 | 0.080 | 3 | 9754859 | missense variant | T/A | snv | 1 | |||
| rs56053615 | 0.851 | 0.120 | 3 | 9751845 | missense variant | G/A;T | snv | 3.4E-04; 4.0E-06 | 4 | ||
| rs1801158 | 0.925 | 0.160 | 1 | 97515865 | missense variant | C/T | snv | 1.5E-02 | 1.4E-02 | 2 | |
| rs104893751 | 0.882 | 0.240 | 3 | 9750423 | missense variant | G/A;C | snv | 2.2E-03; 4.0E-06 | 5 | ||
| rs1801160 | 0.807 | 0.240 | 1 | 97305364 | missense variant | C/T | snv | 4.7E-02 | 3.9E-02 | 6 | |
| rs180040 | 0.882 | 0.120 | 15 | 97027933 | intergenic variant | T/C | snv | 0.85 | 3 | ||
| rs202110856 | 0.790 | 0.080 | 5 | 96794169 | intron variant | -/C | delins | 2.1E-05 | 9 |