Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs657672 | 1.000 | 0.040 | 17 | 39162812 | missense variant | C/T | snv | 0.15 | 0.12 | 1 | |
rs16526 | 1.000 | 0.040 | 17 | 39165419 | non coding transcript exon variant | A/C | snv | 0.20 | 1 | ||
rs16525 | 1.000 | 0.040 | 17 | 39165352 | non coding transcript exon variant | C/T | snv | 0.33 | 1 |