Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1511412 | 1.000 | 0.080 | 3 | 138994862 | regulatory region variant | A/G;T | snv | 1 | |||
rs873549 | 1.000 | 0.080 | 1 | 222098425 | intron variant | C/T | snv | 0.75 | 1 | ||
rs11130248 | 1.000 | 0.080 | 3 | 50314769 | upstream gene variant | A/G | snv | 0.10 | 1 | ||
rs8032158 | 1.000 | 0.080 | 15 | 55902679 | intron variant | T/A;C | snv | 1 | |||
rs1800470 | 0.515 | 0.840 | 19 | 41353016 | missense variant | G/A;C | snv | 0.55; 2.4E-04 | 1 | ||
rs1131691014 | 0.439 | 0.800 | 17 | 7676154 | frameshift variant | -/C | ins | 1 |