Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs869312704 | 0.882 | 0.160 | 2 | 161423752 | frameshift variant | -/GGCTGCA | delins | 10 | |||
rs6265 | 0.436 | 0.760 | 11 | 27658369 | missense variant | C/T | snv | 0.19 | 0.15 | 8 | |
rs1057519511 | 1.000 | 3 | 9734500 | frameshift variant | AG/- | delins | 2 | ||||
rs1057519522 | 1.000 | 10 | 129877788 | stop gained | G/A | snv | 2 | ||||
rs1555349214 | 14 | 36517838 | frameshift variant | G/- | delins | 2 | |||||
rs267606827 | 0.925 | 0.120 | 14 | 28768203 | stop gained | G/A | snv | 1 | |||
rs387906726 | 0.925 | 0.040 | X | 15321727 | stop gained | G/A | snv | 1 | |||
rs145606134 | 0.882 | 0.240 | X | 102937494 | missense variant | A/G | snv | 5.4E-03 | 4.1E-03 | 1 | |
rs17070145 | 0.790 | 0.120 | 5 | 168418786 | intron variant | C/T | snv | 0.43 | 1 |