Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs545854 | 0.882 | 0.160 | 8 | 10002570 | intron variant | G/C | snv | 0.85 | 4 | ||
rs2453626 | 1.000 | 0.080 | 8 | 100125669 | intron variant | T/A;C | snv | 1 | |||
rs1799768 | 0.807 | 0.360 | 7 | 101126425 | upstream gene variant | -/A;C | ins | 6 | |||
rs532966772 | 1.000 | 0.080 | 7 | 101132023 | synonymous variant | C/T | snv | 4.0E-06 | 1 | ||
rs2038366 | 1.000 | 0.080 | 1 | 101235342 | upstream gene variant | G/T | snv | 0.32 | 1 | ||
rs59317557 | 1.000 | 0.080 | 1 | 101236367 | non coding transcript exon variant | C/G | snv | 0.37 | 1 | ||
rs3753194 | 1.000 | 0.080 | 1 | 101237269 | intron variant | A/G | snv | 6.8E-02 | 1 | ||
rs28665122 | 0.807 | 0.240 | 15 | 101277522 | upstream gene variant | C/T | snv | 0.24 | 7 | ||
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 | ||
rs11225138 | 0.925 | 0.200 | 11 | 102123167 | intron variant | G/C | snv | 6.1E-02 | 2 | ||
rs949963 | 0.925 | 0.160 | 2 | 102153326 | intron variant | C/T | snv | 0.22 | 3 | ||
rs871657 | 1.000 | 0.080 | 2 | 102154881 | intron variant | C/T | snv | 0.22 | 2 | ||
rs74180212 | 0.925 | 0.080 | 2 | 102181785 | intron variant | T/C;G | snv | 2 | |||
rs1416580204 | 0.608 | 0.720 | 14 | 102250837 | missense variant | C/T | snv | 4.0E-06 | 7.0E-06 | 49 | |
rs10189629 | 1.000 | 0.080 | 2 | 102263004 | regulatory region variant | C/A | snv | 0.15 | 2 | ||
rs78545931 | 0.925 | 0.080 | 2 | 102265892 | intergenic variant | A/G | snv | 0.16 | 2 | ||
rs11692065 | 1.000 | 0.080 | 2 | 102267515 | intergenic variant | C/T | snv | 0.15 | 2 | ||
rs11674302 | 1.000 | 0.080 | 2 | 102270668 | intergenic variant | T/C | 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 |