Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 264 | |
rs759834365 | 0.448 | 0.760 | 11 | 27658456 | missense variant | C/T | snv | 1.2E-05 | 237 | ||
rs7209436 | 0.851 | 0.200 | 17 | 45792776 | intron variant | C/T | snv | 0.43 | 5 | ||
rs121434622 | 1.000 | 0.080 | X | 147936534 | missense variant | T/A | snv | 2 | |||
rs182830086 | 1.000 | 0.080 | X | 147944892 | missense variant | G/T | snv | 5.5E-06 | 1 |