| Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
|---|---|---|---|---|---|---|---|---|---|---|---|
| rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
| rs2295490 | 0.724 | 0.320 | 20 | 388261 | missense variant | A/G;T | snv | 0.18; 4.0E-06 | 16 | ||
| rs7756992 | 0.827 | 0.240 | 6 | 20679478 | intron variant | A/G;T | snv | 12 | |||
| rs3865188 | 0.790 | 0.320 | 16 | 82617112 | intergenic variant | A/G;T | snv | 10 | |||
| rs56094641 | 0.925 | 0.160 | 16 | 53772541 | intron variant | A/G;T | snv | 4 | |||
| rs3807337 | 1.000 | 0.120 | 7 | 134779071 | intron variant | A/G;T | snv | 1 | |||
| rs4820043 | 1.000 | 0.120 | 22 | 31251108 | intron variant | A/G;T | snv | 1 | |||
| rs11646213 | 0.827 | 0.320 | 16 | 82609046 | intergenic variant | A/T | snv | 0.47 | 6 | ||
| rs3820589 | 0.925 | 0.200 | 1 | 42960373 | intron variant | A/T | snv | 8.3E-02 | 2 | ||
| rs7916840 | 0.925 | 0.160 | 10 | 25424152 | intron variant | A/T | snv | 0.70 | 2 | ||
| rs1129456 | 1.000 | 0.120 | 15 | 32734466 | 3 prime UTR variant | A/T | snv | 0.19 | 1 | ||
| rs17471 | 1.000 | 0.120 | 3 | 120098826 | non coding transcript exon variant | A/T | snv | 6.3E-02 | 1 | ||
| rs3917887 | 0.776 | 0.240 | 17 | 34255979 | non coding transcript exon variant | AGCTCCTCCTTCTC/-;AGCTCCTCCTTCTCAGCTCCTCCTTCTC | delins | 0.33 | 8 | ||
| rs1800630 | 0.701 | 0.480 | 6 | 31574699 | upstream gene variant | C/A | snv | 0.14 | 17 | ||
| rs184003 | 0.724 | 0.400 | 6 | 32182519 | intron variant | C/A | snv | 0.12 | 0.12 | 15 | |
| rs1532624 | 0.851 | 0.160 | 16 | 56971567 | intron variant | C/A | snv | 0.34 | 12 | ||
| rs11915160 | 0.851 | 0.200 | 3 | 181713783 | 3 prime UTR variant | C/A | snv | 0.11 | 5 | ||
| rs7782979 | 0.925 | 0.160 | 7 | 36865445 | intron variant | C/A | snv | 0.46 | 2 | ||
| rs2346061 | 1.000 | 0.120 | 18 | 74533297 | upstream gene variant | C/A | snv | 0.71 | 1 | ||
| rs334543 | 1.000 | 0.120 | 3 | 120113774 | intron variant | C/A | snv | 0.74 | 1 | ||
| rs5749682 | 1.000 | 0.120 | 22 | 33852326 | intron variant | C/A | snv | 0.17 | 1 | ||
| rs1800775 | 0.790 | 0.240 | 16 | 56961324 | upstream gene variant | C/A;G | snv | 0.51; 5.7E-06 | 18 | ||
| rs61758388 | 0.851 | 0.360 | 16 | 17470454 | missense variant | C/A;G | snv | 2.7E-02 | 4 | ||
| rs13254600 | 1.000 | 0.120 | 8 | 123077286 | intron variant | C/A;G | snv | 0.28; 4.8E-06 | 1 | ||
| rs266729 | 0.637 | 0.560 | 3 | 186841685 | upstream gene variant | C/A;G;T | snv | 37 |