Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs7115242 | 0.851 | 0.120 | 11 | 117037567 | intron variant | A/G;T | snv | 16 | |||
rs7190256 | 0.851 | 0.120 | 16 | 72963084 | intron variant | C/T | snv | 0.94 | 16 | ||
rs760762 | 0.851 | 0.120 | 20 | 41147406 | intron variant | C/A;T | snv | 0.59 | 16 | ||
rs2070895 | 0.807 | 0.120 | 15 | 58431740 | intron variant | G/A | snv | 0.33 | 15 | ||
rs2954021 | 1.000 | 0.040 | 8 | 125469835 | intron variant | A/G | snv | 0.54 | 15 | ||
rs6511720 | 0.790 | 0.120 | 19 | 11091630 | intron variant | G/T | snv | 0.12 | 15 | ||
rs157580 | 0.882 | 0.160 | 19 | 44892009 | intron variant | G/A | snv | 0.69 | 14 | ||
rs174576 | 0.851 | 0.200 | 11 | 61836038 | intron variant | C/A;T | snv | 14 | |||
rs2954029 | 0.807 | 0.160 | 8 | 125478730 | intron variant | A/T | snv | 0.42 | 14 | ||
rs673548 | 0.925 | 0.120 | 2 | 21014672 | intron variant | G/A;T | snv | 14 | |||
rs1532085 | 0.882 | 0.080 | 15 | 58391167 | intron variant | A/G;T | snv | 13 | |||
rs174577 | 1.000 | 0.080 | 11 | 61837342 | intron variant | C/A | snv | 0.38 | 13 | ||
rs1883025 | 0.807 | 0.120 | 9 | 104902020 | intron variant | C/T | snv | 0.28 | 13 | ||
rs28601761 | 1.000 | 0.040 | 8 | 125487789 | intron variant | C/G | snv | 0.37 | 13 | ||
rs10468017 | 0.851 | 0.120 | 15 | 58386313 | intron variant | C/T | snv | 0.24 | 12 | ||
rs10846744 | 0.763 | 0.160 | 12 | 124827879 | intron variant | G/C | snv | 0.32 | 11 | ||
rs174570 | 0.882 | 0.200 | 11 | 61829740 | intron variant | C/T | snv | 0.15 | 11 | ||
rs2247056 | 0.882 | 0.160 | 6 | 31297713 | intron variant | T/C | snv | 0.80 | 11 | ||
rs1128249 | 1.000 | 0.080 | 2 | 164672114 | intron variant | G/C;T | snv | 10 | |||
rs1864163 | 0.882 | 0.120 | 16 | 56963321 | intron variant | G/A | snv | 0.26 | 10 | ||
rs2068834 | 0.925 | 0.120 | 2 | 27616672 | intron variant | T/C | snv | 0.28 | 10 | ||
rs2075290 | 0.882 | 0.160 | 11 | 116782580 | intron variant | C/G;T | snv | 10 | |||
rs2925979 | 1.000 | 0.080 | 16 | 81501185 | intron variant | T/A;C | snv | 10 | |||
rs516246 | 0.925 | 0.160 | 19 | 48702915 | intron variant | C/T | snv | 0.38 | 0.45 | 10 | |
rs6589566 | 0.882 | 0.080 | 11 | 116781707 | intron variant | G/A;C;T | snv | 10 |