Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2253612 | 1.000 | 0.080 | 2 | 200703710 | intron variant | C/T | snv | 0.79 | 3 | ||
rs2540051 | 2 | 200706420 | splice donor variant | G/A | snv | 0.22 | 1 | ||||
rs7563911 | 2 | 200711561 | non coding transcript exon variant | A/C;G;T | snv | 1 | |||||
rs2348114 | 2 | 200717470 | non coding transcript exon variant | T/C | snv | 0.82 | 1 | ||||
rs7589014 | 2 | 200716231 | intron variant | C/T | snv | 0.11 | 1 |