Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs57105105 | 0.925 | 0.080 | 8 | 24953776 | missense variant | C/T | snv | 4 | |||
rs201059543 | 12 | 121184366 | missense variant | C/G;T | snv | 4.0E-06; 3.6E-05 | 2 | ||||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 272 |