Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4680 | 0.442 | 0.920 | 22 | 19963748 | missense variant | G/A | snv | 0.46 | 0.44 | 249 | |
rs1045642 | 0.456 | 0.840 | 7 | 87509329 | synonymous variant | A/G;T | snv | 0.50 | 214 | ||
rs2032582 | 0.538 | 0.800 | 7 | 87531302 | missense variant | A/C;T | snv | 0.54; 3.8E-02 | 97 | ||
rs1799971 | 0.559 | 0.600 | 6 | 154039662 | missense variant | A/G | snv | 0.19 | 0.12 | 95 | |
rs324420 | 0.637 | 0.440 | 1 | 46405089 | missense variant | C/A | snv | 0.24 | 0.26 | 48 | |
rs4633 | 0.695 | 0.400 | 22 | 19962712 | synonymous variant | C/T | snv | 0.46 | 0.45 | 25 | |
rs7439366 | 0.752 | 0.320 | 4 | 69098620 | missense variant | T/C | snv | 0.56 | 0.57 | 16 | |
rs769540300 | 0.851 | 0.200 | 6 | 154091047 | missense variant | G/A | snv | 1.2E-05 | 8 | ||
rs765502022 | 0.827 | 0.240 | 4 | 69112695 | missense variant | T/C | snv | 1.6E-05 | 8 | ||
rs8007267 | 0.882 | 0.200 | 14 | 54912273 | intergenic variant | C/T | snv | 0.31 | 6 | ||
rs1718125 | 0.851 | 0.200 | 12 | 121155216 | intron variant | C/T | snv | 0.15 | 0.19 | 6 | |
rs373611092 | 0.925 | 0.160 | 22 | 19962794 | missense variant | A/G | snv | 8.4E-05 | 4.9E-05 | 5 | |
rs2234918 | 0.827 | 0.200 | 1 | 28863085 | synonymous variant | C/T | snv | 0.59 | 0.50 | 5 | |
rs3783641 | 0.882 | 0.120 | 14 | 54893421 | intron variant | T/A;C | snv | 0.25 | 4 | ||
rs2835859 | 0.925 | 0.200 | 21 | 37645860 | intron variant | T/C | snv | 0.16 | 3 | ||
rs533123 | 0.882 | 0.160 | 1 | 28814643 | intron variant | G/A;C | snv | 3 | |||
rs13093031 | 1.000 | 0.120 | 3 | 88809891 | intergenic variant | A/G | snv | 0.17 | 2 | ||
rs6961071 | 1.000 | 0.120 | 7 | 156182007 | downstream gene variant | A/G;T | snv | 0.47 | 2 | ||
rs1288779666 | 1.000 | 0.120 | 22 | 42128944 | missense variant | C/G | snv | 2 | |||
rs76060075 | 1.000 | 0.120 | 22 | 42129185 | missense variant | C/G | snv | 2 | |||
rs749415280 | 1.000 | 0.120 | 4 | 69096638 | missense variant | A/G | snv | 2 | |||
rs10483636 | 1.000 | 0.120 | 14 | 54334127 | intergenic variant | A/G | snv | 7.2E-02 | 1 | ||
rs1473203326 | 1.000 | 0.120 | 22 | 42128215 | missense variant | G/A | snv | 1 | |||
rs1187761291 | 1.000 | 0.120 | 6 | 154039569 | missense variant | A/G | snv | 4.1E-06 | 1 | ||
rs200811844 | 1.000 | 0.120 | 6 | 154091110 | missense variant | T/C | snv | 1.8E-04 | 7.8E-04 | 1 |