Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6091189 | 0.776 | 0.080 | 20 | 50639748 | intron variant | C/T | snv | 0.25 | 10 | ||
rs914458 | 0.925 | 0.080 | 20 | 50594416 | intron variant | G/C | snv | 0.23 | 2 | ||
rs1060402 | 20 | 50588558 | intron variant | G/A | snv | 0.45 | 1 | ||||
rs117246187 | 20 | 50690397 | intron variant | A/G | snv | 5.7E-02 | 1 |