| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs142883642 | 1.000 | 0.040 | 2 | 208248486 | missense variant | T/C | snv | 3.6E-05 | 2.1E-05 | 2 | |
| rs1525892 | 1.000 | 0.040 | 3 | 133765868 | intron variant | G/A;T | snv | 2 | |||
| rs1541580 | 1.000 | 0.040 | 2 | 64994050 | intron variant | C/T | snv | 0.77 | 2 | ||
| rs1559715 | 1.000 | 0.040 | 4 | 54207506 | intron variant | G/A | snv | 0.20 | 2 | ||
| rs1635183 | 1.000 | 0.040 | 7 | 11643752 | intron variant | C/A;G | snv | 2 | |||
| rs16840314 | 1.000 | 0.040 | 1 | 158547563 | synonymous variant | G/A | snv | 0.23 | 0.19 | 2 | |
| rs16891264 | 1.000 | 0.040 | 6 | 26072217 | intergenic variant | T/C | snv | 9.0E-02 | 2 | ||
| rs17093914 | 1.000 | 0.040 | 14 | 74896938 | intron variant | C/G;T | snv | 2 | |||
| rs17109512 | 1.000 | 0.040 | 10 | 98367794 | regulatory region variant | G/A | snv | 9.5E-02 | 2 | ||
| rs17109634 | 1.000 | 0.040 | 10 | 98396036 | intron variant | C/T | snv | 5.2E-02 | 2 | ||
| rs17399603 | 1.000 | 0.040 | 3 | 101017295 | regulatory region variant | A/G | snv | 0.10 | 2 | ||
| rs183484 | 0.925 | 0.040 | 11 | 4119902 | synonymous variant | C/A | snv | 0.45 | 0.39 | 2 | |
| rs2023454 | 1.000 | 0.040 | 20 | 54650572 | 3 prime UTR variant | C/G | snv | 0.13 | 2 | ||
| rs2147897 | 1.000 | 0.040 | 10 | 98388056 | non coding transcript exon variant | G/T | snv | 0.45 | 2 | ||
| rs2241107 | 1.000 | 0.040 | 1 | 156212919 | upstream gene variant | T/C;G | snv | 2 | |||
| rs2243834 | 1.000 | 0.040 | 2 | 26134879 | intron variant | G/C;T | snv | 2 | |||
| rs2253677 | 1.000 | 0.040 | 1 | 156201505 | intron variant | C/G | snv | 0.42 | 2 | ||
| rs2268276 | 0.925 | 0.040 | 21 | 34808717 | intron variant | G/A | snv | 0.38 | 2 | ||
| rs2274248 | 1.000 | 0.040 | 10 | 98388785 | intron variant | C/T | snv | 0.27 | 2 | ||
| rs2274249 | 1.000 | 0.040 | 10 | 98388658 | intron variant | C/T | snv | 5.7E-02 | 2 | ||
| rs2282015 | 1.000 | 0.040 | 10 | 123462521 | intron variant | T/G | snv | 0.39 | 2 | ||
| rs2304205 | 0.925 | 0.040 | 19 | 49665670 | splice donor variant | A/C;T | snv | 0.36 | 2 | ||
| rs2393726 | 0.925 | 0.040 | 10 | 62094648 | 3 prime UTR variant | A/G | snv | 3.9E-02 | 2 | ||
| rs2452877 | 1.000 | 0.040 | 5 | 4027643 | regulatory region variant | A/G | snv | 0.60 | 2 | ||
| rs2562456 | 1.000 | 0.040 | 19 | 21483408 | non coding transcript exon variant | C/T | snv | 0.77 | 2 |