Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800629 | 0.472 | 0.920 | 6 | 31575254 | upstream gene variant | G/A | snv | 0.12 | 0.14 | 169 | |
rs1800890 | 0.658 | 0.400 | 1 | 206776020 | intron variant | A/T | snv | 0.32 | 29 | ||
rs1057519825 | 0.882 | 0.120 | X | 101356176 | missense variant | C/G | snv | 7 | |||
rs1057519826 | 0.882 | 0.120 | X | 101356177 | missense variant | A/T | snv | 7 | |||
rs2509049 | 0.827 | 0.160 | 11 | 119095811 | upstream gene variant | C/A;T | snv | 6 | |||
rs604714 | 0.925 | 0.120 | 11 | 119099986 | intron variant | C/A | snv | 0.31 | 3 | ||
rs121434222 | 0.925 | 0.280 | 11 | 108287687 | stop gained | C/T | snv | 2 | |||
rs121434221 | 1.000 | 0.120 | 11 | 108329199 | missense variant | A/G | snv | 1 | |||
rs796051857 | 1.000 | 0.120 | 11 | 108329181 | inframe insertion | -/GAA | delins | 1 |