Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs13022699 | 1.000 | 0.080 | 2 | 101671373 | intergenic variant | C/T | snv | 5.3E-02 | 1 | ||
rs12468899 | 1.000 | 0.080 | 2 | 101809678 | intron variant | A/G;T | snv | 1 | |||
rs1709393 | 1.000 | 0.080 | 3 | 101980310 | intron variant | C/T | snv | 0.55 | 2 | ||
rs13427957 | 1.000 | 0.080 | 2 | 102072571 | intron variant | C/T | snv | 0.46 | 1 | ||
rs74180212 | 0.925 | 0.080 | 2 | 102181785 | intron variant | T/C;G | snv | 2 | |||
rs10189629 | 1.000 | 0.080 | 2 | 102263004 | regulatory region variant | C/A | snv | 0.15 | 1 | ||
rs78545931 | 0.925 | 0.080 | 2 | 102265892 | intergenic variant | A/G | snv | 0.16 | 2 | ||
rs60227565 | 0.925 | 0.080 | 2 | 102275879 | intergenic variant | G/A;T | snv | 0.10 | 2 | ||
rs202011557 | 1.000 | 0.080 | 2 | 102297182 | intergenic variant | -/CAA | delins | 1 | |||
rs10515922 | 1.000 | 0.080 | 2 | 102298194 | regulatory region variant | A/G | snv | 6.9E-02 | 1 | ||
rs12470864 | 0.925 | 0.080 | 2 | 102309902 | upstream gene variant | G/A | snv | 0.30 | 4 | ||
rs72823641 | 0.882 | 0.080 | 2 | 102319699 | intron variant | T/A;C | snv | 4 | |||
rs12479210 | 1.000 | 0.080 | 2 | 102332701 | intron variant | C/A;T | snv | 1 | |||
rs3771180 | 1.000 | 0.080 | 2 | 102337157 | 5 prime UTR variant | G/A;T | snv | 1 | |||
rs13408661 | 1.000 | 0.080 | 2 | 102338622 | intron variant | G/A | snv | 0.18 | 1 | ||
rs1420101 | 0.827 | 0.280 | 2 | 102341256 | synonymous variant | C/T | snv | 0.33 | 0.35 | 3 | |
rs3771175 | 0.925 | 0.080 | 2 | 102343750 | 3 prime UTR variant | T/A | snv | 0.18 | 1 | ||
rs10208293 | 0.882 | 0.160 | 2 | 102349850 | intron variant | G/A | snv | 0.33 | 2 | ||
rs10197862 | 0.925 | 0.120 | 2 | 102350089 | intron variant | A/G | snv | 0.18 | 2 | ||
rs1861245 | 0.925 | 0.080 | 2 | 102350446 | intron variant | C/T | snv | 2 | |||
rs9807989 | 1.000 | 0.080 | 2 | 102354740 | intron variant | T/C;G | snv | 0.46 | 2 | ||
rs3771166 | 1.000 | 0.080 | 2 | 102369762 | intron variant | G/A;T | snv | 1 | |||
rs2241116 | 1.000 | 0.080 | 2 | 102386805 | intron variant | C/A;T | snv | 1 | |||
rs917997 | 0.701 | 0.480 | 2 | 102454108 | downstream gene variant | T/A;C | snv | 2 | |||
rs227283 | 0.925 | 0.120 | 4 | 102686096 | intron variant | C/G;T | snv | 2 |