| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs1217691063 | 0.330 | 0.920 | 1 | 11796309 | missense variant | A/G | snv | 4.0E-06 | 7.0E-06 | 614 | |
| rs121913279 | 0.526 | 0.560 | 3 | 179234297 | missense variant | A/G;T | snv | 4.0E-06; 4.0E-06 | 101 | ||
| rs2228145 | 0.602 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 0.38; 1.2E-05 | 57 | ||
| rs4647924 | 0.600 | 0.520 | 4 | 1801844 | missense variant | C/A;G;T | snv | 4.2E-06; 4.2E-06 | 49 | ||
| rs121912664 | 0.630 | 0.320 | 17 | 7670699 | missense variant | C/A;G;T | snv | 1.2E-05 | 44 | ||
| rs1800797 | 0.605 | 0.800 | 7 | 22726602 | non coding transcript exon variant | A/G | snv | 0.72 | 43 | ||
| rs8192284 | 0.724 | 0.720 | 1 | 154454494 | missense variant | A/C;T | snv | 19 | |||
| rs80356616 | 0.732 | 0.360 | 11 | 17387917 | missense variant | C/T | snv | 19 | |||
| rs2165241 | 0.716 | 0.360 | 15 | 73929861 | intron variant | T/C | snv | 0.60 | 15 | ||
| rs3825942 | 0.716 | 0.320 | 15 | 73927241 | missense variant | G/A;C;T | snv | 0.18; 4.5E-06 | 15 | ||
| rs1285524167 | 0.807 | 0.280 | 11 | 17475004 | missense variant | C/T | snv | 8.0E-06 | 8 | ||
| rs104893810 | 0.790 | 0.360 | 3 | 30691477 | missense variant | C/T | snv | 7 | |||
| rs1057518972 | 0.827 | 0.200 | 8 | 115418359 | missense variant | C/T | snv | 7 | |||
| rs1524107 | 0.827 | 0.320 | 7 | 22728600 | non coding transcript exon variant | C/T | snv | 9.4E-02 | 6 | ||
| rs180349 | 0.925 | 0.200 | 11 | 116741111 | intergenic variant | A/C;T | snv | 5 | |||
| rs121912974 | 0.882 | 0.240 | 7 | 75983548 | missense variant | G/C | snv | 2.4E-04 | 2.2E-04 | 4 | |
| rs228503 | 0.882 | 0.200 | 1 | 79217216 | intron variant | T/C | snv | 0.42 | 3 | ||
| rs201405525 | 0.925 | 0.240 | 8 | 90044993 | missense variant | G/A;C | snv | 4.5E-04; 4.0E-06 | 3 | ||
| rs9333649 | 0.882 | 0.200 | 7 | 150951679 | missense variant | C/A;G;T | snv | 3 | |||
| rs11696257 | 0.882 | 0.240 | 20 | 40642176 | regulatory region variant | C/T | snv | 0.36 | 3 | ||
| rs6445834 | 0.925 | 0.200 | 3 | 56881691 | intron variant | T/C | snv | 0.64 | 2 | ||
| rs387906539 | 0.925 | 0.280 | 19 | 7184592 | missense variant | A/G | snv | 2 | |||
| rs199472743 | 0.925 | 0.200 | 11 | 2583439 | missense variant | C/G;T | snv | 2 | |||
| rs6065259 | 0.925 | 0.200 | 20 | 40633339 | intergenic variant | G/A | snv | 0.38 | 2 | ||
| rs1131690998 | 0.925 | 0.280 | 9 | 95506484 | missense variant | A/C | snv | 2 |