Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1840680 | 0.807 | 0.200 | 3 | 157438240 | intron variant | A/G | snv | 0.59 | 6 | ||
rs368060 | 0.882 | 0.200 | 1 | 155235217 | missense variant | C/G | snv | 1.4E-04 | 7.7E-04 | 3 | |
rs4986790 | 0.438 | 0.800 | 9 | 117713024 | missense variant | A/G;T | snv | 6.1E-02; 4.0E-06 | 223 | ||
rs76763715 | 0.658 | 0.520 | 1 | 155235843 | missense variant | T/C;G | snv | 2.3E-03 | 35 |