Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1554389088 | 0.807 | 0.160 | 7 | 44243526 | missense variant | G/A | snv | 27 | |||
rs1554386687 | 0.882 | 0.040 | 7 | 44242328 | missense variant | C/T | snv | 12 | |||
rs926027867 | 0.882 | 0.040 | 5 | 150251808 | missense variant | G/A;T | snv | 12 | |||
rs1287121256 | 0.882 | 0.040 | 5 | 150256777 | missense variant | C/G;T | snv | 7.0E-06 | 9 | ||
rs1554122526 | 0.882 | 0.040 | 5 | 150256811 | missense variant | A/G | snv | 9 | |||
rs1554123982 | 0.925 | 0.040 | 5 | 150273157 | splice acceptor variant | C/- | delins | 7 |