Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1799810 | 1.000 | 0.040 | 2 | 127418464 | 5 prime UTR variant | A/T | snv | 0.38 | 0.44 | 5 | |
rs10485505 | 1.000 | 0.080 | 20 | 34437762 | intron variant | C/G;T | snv | 3 | |||
rs1158867 | 1.000 | 0.080 | 2 | 127419801 | splice region variant | C/T | snv | 0.51 | 3 | ||
rs1799808 | 1.000 | 0.040 | 2 | 127418286 | upstream gene variant | C/T | snv | 0.33 | 3 | ||
rs1885119 | 1.000 | 0.080 | 20 | 35057846 | intron variant | T/C | snv | 0.58 | 3 | ||
rs2065108 | 1.000 | 0.080 | 20 | 35119019 | intron variant | C/T | snv | 0.61 | 3 | ||
rs3736802 | 1.000 | 0.080 | 20 | 35016239 | intron variant | T/C | snv | 0.53 | 3 | ||
rs3818253 | 1.000 | 0.040 | 20 | 35009073 | intron variant | G/A | snv | 0.19 | 3 | ||
rs4150407 | 1.000 | 0.120 | 2 | 127292055 | 3 prime UTR variant | T/C | snv | 0.47 | 3 | ||
rs6060038 | 1.000 | 0.080 | 20 | 34769912 | intron variant | G/A | snv | 0.45 | 3 | ||
rs6087664 | 1.000 | 0.080 | 20 | 35038413 | intron variant | C/A;G;T | snv | 3 | |||
rs6088343 | 1.000 | 0.040 | 20 | 33908259 | downstream gene variant | C/T | snv | 0.46 | 3 | ||
rs6088590 | 1.000 | 0.040 | 20 | 34725762 | intron variant | T/C | snv | 0.36 | 3 | ||
rs6088662 | 1.000 | 0.040 | 20 | 34959830 | intron variant | T/G | snv | 0.20 | 3 | ||
rs6088692 | 1.000 | 0.080 | 20 | 35050785 | intron variant | A/G | snv | 0.58 | 3 | ||
rs6088727 | 1.000 | 0.080 | 20 | 35125836 | intron variant | G/A | snv | 0.51 | 3 | ||
rs6120816 | 1.000 | 0.080 | 20 | 35056555 | intron variant | G/A;C | snv | 3 | |||
rs6141509 | 1.000 | 0.080 | 20 | 34731584 | intron variant | G/A | snv | 0.45 | 3 | ||
rs6142044 | 1.000 | 0.040 | 20 | 33918789 | intergenic variant | A/T | snv | 0.47 | 3 | ||
rs2068834 | 0.925 | 0.120 | 2 | 27616672 | intron variant | T/C | snv | 0.28 | 10 | ||
rs1178977 | 0.925 | 0.120 | 7 | 73442719 | splice region variant | A/G | snv | 0.16 | 0.21 | 7 | |
rs7811265 | 0.925 | 0.120 | 7 | 73520180 | intron variant | A/G | snv | 0.23 | 7 | ||
rs1178979 | 0.925 | 0.120 | 7 | 73442100 | 3 prime UTR variant | T/C | snv | 0.21 | 6 | ||
rs17145713 | 0.925 | 0.120 | 7 | 73490480 | intron variant | C/T | snv | 0.21 | 6 | ||
rs1919127 | 0.925 | 0.120 | 2 | 27578626 | missense variant | T/C | snv | 0.31 | 0.27 | 6 |