Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs142529006 | 7 | 100022093 | intron variant | T/A | snv | 6.9E-03 | 4 | ||||
rs9487023 | 6 | 109268801 | intron variant | A/G | snv | 0.40 | 8 | ||||
rs79674254 | 6 | 109501078 | intron variant | C/A;T | snv | 3 | |||||
rs888194 | 12 | 109549113 | downstream gene variant | C/G | snv | 0.50 | 3 | ||||
rs754205 | 13 | 109759295 | intron variant | A/C;G | snv | 4 | |||||
rs35188965 | 5 | 1104823 | intron variant | C/G;T | snv | 12 | |||||
rs2009581 | 2 | 111050100 | intron variant | G/A | snv | 0.26 | 3 | ||||
rs148125759 | 9 | 111901105 | intron variant | T/C | snv | 1.0E-02 | 4 | ||||
rs368865 | 13 | 112825506 | missense variant | A/C;G;T | snv | 0.76; 4.0E-06 | 4 | ||||
rs55709272 | 2 | 113109711 | intron variant | T/A;C | snv | 5 | |||||
rs56129102 | 13 | 113220766 | intron variant | C/T | snv | 0.20 | 3 | ||||
rs1169299 | 1.000 | 0.080 | 12 | 120991391 | intron variant | T/C | snv | 0.43 | 4 | ||
rs9423289 | 10 | 122945179 | intron variant | C/T | snv | 0.58 | 3 | ||||
rs532591337 | 19 | 12459271 | intron variant | G/A | snv | 4.9E-05 | 4 | ||||
rs28601761 | 1.000 | 0.040 | 8 | 125487789 | intron variant | C/G | snv | 0.37 | 13 | ||
rs11244669 | 10 | 125844213 | intron variant | A/C | snv | 0.28 | 4 | ||||
rs57565032 | 12 | 131949846 | upstream gene variant | G/T | snv | 0.14 | 4 | ||||
rs8177318 | 3 | 133748533 | missense variant | T/A | snv | 1.6E-04 | 2.9E-04 | 7 | |||
rs7775698 | 1.000 | 0.080 | 6 | 135097497 | intron variant | C/T | snv | 6.9E-02 | 14 | ||
rs7776054 | 6 | 135097778 | intron variant | A/G | snv | 0.24 | 13 | ||||
rs73713131 | 8 | 140448235 | intron variant | T/C | snv | 8.8E-02 | 3 | ||||
rs1050828 | 0.790 | 0.200 | X | 154536002 | missense variant | C/T | snv | 9.1E-03 | 3.6E-02 | 15 | |
rs706027 | 7 | 16660352 | intron variant | A/T | snv | 0.43 | 4 | ||||
rs183034862 | 2 | 168457008 | intron variant | C/T | snv | 1.8E-02 | 3 | ||||
rs116577908 | 3 | 17056907 | intron variant | A/G | snv | 7.1E-03 | 4 |