Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs56205728 | 1.000 | 0.040 | 15 | 40275036 | intron variant | G/A | snv | 0.26 | 1 | ||
rs56282503 | 1.000 | 0.040 | 15 | 40274558 | intron variant | T/C | snv | 0.21 | 1 |