Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs3184504 | 0.572 | 0.600 | 12 | 111446804 | missense variant | T/A;C;G | snv | 0.67 | 92 | ||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 81 | |
rs1047891 | 0.827 | 0.200 | 2 | 210675783 | missense variant | C/A | snv | 0.30 | 0.33 | 34 | |
rs1800961 | 0.851 | 0.160 | 20 | 44413724 | missense variant | C/T | snv | 3.1E-02 | 2.5E-02 | 21 | |
rs2954021 | 1.000 | 0.040 | 8 | 125469835 | intron variant | A/G | snv | 0.54 | 15 | ||
rs998584 | 6 | 43790159 | downstream gene variant | C/A | snv | 0.41 | 11 | ||||
rs333947 | 1 | 109928142 | intron variant | G/A | snv | 0.13 | 7 | ||||
rs13135092 | 4 | 102276925 | intron variant | A/G | snv | 5.1E-02 | 4 | ||||
rs72836561 | 17 | 43848758 | missense variant | C/T | snv | 2.2E-02 | 2.0E-02 | 4 | |||
rs4805881 | 19 | 33405526 | intron variant | A/C | snv | 0.69 | 3 | ||||
rs2494748 | 14 | 104792555 | intron variant | C/T | snv | 0.51 | 0.48 | 2 |