Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1567190244 | 1.000 | 16 | 2108041 | intron variant | C/T | snv | 1 | ||||
rs1616940 | 0.925 | 0.120 | 16 | 2114843 | missense variant | A/G;T | snv | 2 | |||
rs199476100 | 0.925 | 0.120 | 16 | 2114489 | missense variant | A/G | snv | 4.3E-06 | 2 | ||
rs770519542 | 0.925 | 11 | 62630788 | missense variant | C/A;T | snv | 4.0E-06 | 2 | |||
rs879255642 | 0.925 | 11 | 62631032 | missense variant | G/C | snv | 2 | ||||
rs879255643 | 0.925 | 11 | 62626633 | missense variant | G/A | snv | 2 | ||||
rs1567187420 | 1.000 | 16 | 2106903 | frameshift variant | C/- | del | 1 | ||||
rs1567195868 | 1.000 | 16 | 2109473 | frameshift variant | -/A | delins | 1 | ||||
rs879255641 | 1.000 | 11 | 62629281 | frameshift variant | CT/- | del | 1 |