Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1801282 | 0.500 | 0.840 | 3 | 12351626 | missense variant | C/G | snv | 0.11 | 8.9E-02 | 131 | |
rs1805192 | 0.510 | 0.840 | 3 | 12379739 | missense variant | C/G | snv | 121 | |||
rs3816873 | 0.790 | 0.200 | 4 | 99583507 | missense variant | T/C | snv | 0.25 | 0.26 | 9 | |
rs33957861 | 0.882 | 0.160 | 10 | 67887218 | intron variant | C/T | snv | 0.11 | 3 | ||
rs11599176 | 0.925 | 0.080 | 10 | 67894017 | intron variant | A/G | snv | 0.11 | 2 | ||
rs35689145 | 1.000 | 0.080 | 10 | 67900009 | intron variant | G/A;C | snv | 1 |