Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs10511729 | 0.742 | 0.240 | 9 | 23557229 | intron variant | T/G | snv | 0.35 | 11 | ||
rs12683422 | 0.742 | 0.240 | 9 | 27969442 | intron variant | C/T | snv | 5.7E-02 | 11 | ||
rs16901904 | 0.790 | 0.160 | 8 | 127015257 | intron variant | T/C | snv | 0.27 | 7 | ||
rs1799750 | 0.592 | 0.760 | 11 | 102799765 | intron variant | C/- | delins | 0.50 | 48 | ||
rs2070584 | 0.790 | 0.200 | X | 47587120 | intron variant | T/G | snv | 0.44 | 8 | ||
rs2075685 | 0.724 | 0.320 | 5 | 83076846 | intron variant | G/A;T | snv | 14 | |||
rs2075686 | 0.742 | 0.240 | 5 | 83076927 | intron variant | C/T | snv | 1.7E-02 | 13 | ||
rs2107425 | 0.732 | 0.280 | 11 | 1999845 | intron variant | C/T | snv | 16 | |||
rs28360071 | 0.708 | 0.240 | 5 | 83142293 | intron variant | GATGAGGAAACTAACTCTCAGTGGTGTTTA/- | delins | 0.48 | 18 | ||
rs28360317 | 0.716 | 0.280 | 5 | 83323739 | intron variant | -/CCT | delins | 0.24 | 15 | ||
rs2854509 | 0.807 | 0.160 | 19 | 43570445 | intron variant | T/G | snv | 0.80 | 6 | ||
rs3136817 | 0.732 | 0.280 | 14 | 20456275 | intron variant | T/C | snv | 0.23 | 12 | ||
rs3731239 | 0.763 | 0.240 | 9 | 21974219 | intron variant | A/G | snv | 0.26 | 10 | ||
rs3740393 | 0.776 | 0.280 | 10 | 102876898 | intron variant | G/C;T | snv | 10 | |||
rs3757441 | 0.752 | 0.200 | 7 | 148827660 | intron variant | C/T | snv | 0.80 | 12 | ||
rs401681 | 0.620 | 0.640 | 5 | 1321972 | intron variant | C/T | snv | 0.48 | 42 | ||
rs4957014 | 0.752 | 0.160 | 5 | 287899 | intron variant | T/G | snv | 0.74 | 11 | ||
rs6869366 | 0.701 | 0.280 | 5 | 83075927 | intron variant | T/G | snv | 9.2E-02 | 18 | ||
rs7003908 | 0.716 | 0.320 | 8 | 47858141 | intron variant | C/A | snv | 0.66 | 16 | ||
rs710886 | 0.763 | 0.160 | 8 | 127014615 | intron variant | C/T | snv | 0.37 | 9 | ||
rs762551 | 0.701 | 0.400 | 15 | 74749576 | intron variant | C/A | snv | 0.67 | 23 | ||
rs7727691 | 0.763 | 0.200 | 5 | 83075876 | intron variant | C/T | snv | 0.32 | 9 | ||
rs8034191 | 0.695 | 0.440 | 15 | 78513681 | intron variant | T/C | snv | 0.27 | 24 | ||
rs10811474 | 0.742 | 0.240 | 9 | 21114238 | intergenic variant | A/G | snv | 0.44 | 11 | ||
rs13181 | 0.487 | 0.760 | 19 | 45351661 | stop gained | T/A;G | snv | 4.0E-06; 0.32 | 134 |