Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1800796 | 0.555 | 0.760 | 7 | 22726627 | non coding transcript exon variant | G/C | snv | 9.9E-02 | 74 | ||
rs1345176461 | 0.716 | 0.240 | 14 | 77027231 | stop gained | G/A;T | snv | 4.3E-06 | 40 | ||
rs2069837 | 0.724 | 0.520 | 7 | 22728408 | intron variant | A/C;G | snv | 18 | |||
rs61751362 | 0.790 | 0.160 | X | 154030948 | stop gained | G/A;C | snv | 1.6E-05 | 14 | ||
rs730882246 | 0.807 | 0.200 | 14 | 74494329 | missense variant | G/A | snv | 8 | |||
rs1569324457 | 0.851 | 0.280 | 20 | 32433481 | frameshift variant | AG/- | del | 7 | |||
rs3782219 | 1.000 | 0.080 | 12 | 117350435 | intron variant | C/T | snv | 0.17 | 1 |