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 | 61 | ||
rs1260326 | 0.645 | 0.600 | 2 | 27508073 | missense variant | T/C;G | snv | 0.63; 4.0E-06 | 0.68 | 55 | |
rs671 | 0.529 | 0.840 | 12 | 111803962 | missense variant | G/A | snv | 1.9E-02 | 5.8E-03 | 21 | |
rs1182188 | 0.827 | 0.120 | 7 | 2830351 | intron variant | T/C | snv | 0.26 | 7 | ||
rs34517439 | 0.882 | 0.120 | 1 | 77984833 | intron variant | C/A | snv | 7.3E-02 | 7 | ||
rs35874463 | 0.827 | 0.120 | 15 | 67165360 | missense variant | A/G | snv | 4.0E-02 | 3.4E-02 | 7 | |
rs2066807 | 0.925 | 0.080 | 12 | 56346898 | missense variant | C/G | snv | 4.9E-02 | 4.6E-02 | 2 | |
rs2066808 | 0.807 | 0.280 | 12 | 56344189 | intron variant | A/G | snv | 0.21 | 2 | ||
rs2778031 | 1.000 | 0.040 | 9 | 88220811 | intergenic variant | T/A;C | snv | 2 |