Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1801275 | 0.581 | 0.680 | 16 | 27363079 | missense variant | A/G | snv | 0.25 | 0.36 | 58 | |
rs20541 | 0.585 | 0.720 | 5 | 132660272 | missense variant | A/G | snv | 0.72 | 0.77 | 52 | |
rs2569190 | 0.620 | 0.560 | 5 | 140633331 | intron variant | A/G | snv | 0.57 | 39 | ||
rs759191907 | 0.776 | 0.360 | 9 | 127825225 | splice region variant | A/G | snv | 8.0E-06 | 25 | ||
rs5743810 | 0.689 | 0.360 | 4 | 38828729 | missense variant | A/G | snv | 0.73 | 0.72 | 21 | |
rs10993994 | 0.763 | 0.280 | 10 | 46046326 | 5 prime UTR variant | A/G | snv | 0.54 | 15 | ||
rs6894249 | 0.776 | 0.160 | 5 | 132461855 | non coding transcript exon variant | A/G | snv | 0.45 | 9 | ||
rs569108 | 0.790 | 0.200 | 11 | 60095631 | missense variant | A/G | snv | 4.7E-02 | 7.3E-02 | 8 | |
rs1295685 | 0.790 | 0.160 | 5 | 132660753 | 3 prime UTR variant | A/G | snv | 0.81 | 7 | ||
rs479844 | 0.851 | 0.160 | 11 | 65784486 | upstream gene variant | A/G | snv | 0.44 | 6 | ||
rs2158177 | 0.925 | 0.120 | 5 | 132648366 | intron variant | A/G | snv | 0.18 | 5 | ||
rs2303067 | 0.851 | 0.160 | 5 | 148101392 | missense variant | A/G | snv | 0.52 | 0.44 | 5 | |
rs9357733 | 0.851 | 0.160 | 6 | 52427338 | intron variant | A/G | snv | 0.19 | 4 | ||
rs13277355 | 0.882 | 0.120 | 8 | 127765473 | intergenic variant | A/G | snv | 0.71 | 3 | ||
rs13360927 | 0.882 | 0.160 | 5 | 110700055 | intron variant | A/G | snv | 9.3E-02 | 3 | ||
rs7518129 | 0.882 | 0.120 | 1 | 173194429 | intron variant | A/G | snv | 0.47 | 3 | ||
rs11204971 | 0.925 | 0.120 | 1 | 152286602 | intron variant | A/G | snv | 0.15 | 2 | ||
rs112111458 | 0.925 | 0.120 | 2 | 70872975 | intergenic variant | A/G | snv | 0.16 | 2 | ||
rs17718511 | 0.925 | 0.120 | 5 | 148072009 | intron variant | A/G | snv | 3.2E-02 | 2 | ||
rs2066446 | 0.925 | 0.120 | 1 | 67315434 | intron variant | A/G | snv | 0.20 | 2 | ||
rs28441202 | 0.925 | 0.120 | 1 | 152156387 | missense variant | A/G | snv | 2 | |||
rs3756094 | 0.925 | 0.120 | 4 | 184429780 | intron variant | A/G | snv | 0.66 | 2 | ||
rs4580194 | 1.000 | 0.040 | 17 | 39970224 | intron variant | A/G | snv | 0.41 | 2 | ||
rs5029949 | 0.925 | 0.120 | 6 | 137876369 | intron variant | A/G | snv | 8.1E-02 | 2 | ||
rs10468514 | 1.000 | 0.040 | 17 | 45378874 | intergenic variant | A/G | snv | 0.38 | 1 |