Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1801133 | 0.472 | 0.880 | 1 | 11796321 | missense variant | G/A | snv | 0.31 | 0.27 | 174 | |
rs1801222 | 0.925 | 0.160 | 10 | 17114152 | missense variant | A/G | snv | 0.73 | 0.72 | 5 | |
rs10986018 | 9 | 98361054 | intron variant | T/C | snv | 7.9E-02 | 2 | ||||
rs12085006 | 1 | 11898666 | intergenic variant | A/G;T | snv | 2 |