Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4812833 | 0.827 | 0.120 | 20 | 44440356 | intron variant | G/A;C | snv | 5 | |||
rs6017342 | 0.925 | 0.120 | 20 | 44436388 | non coding transcript exon variant | A/C | snv | 0.62 | 2 | ||
rs6073450 | 1.000 | 0.120 | 20 | 44458008 | intron variant | G/A | snv | 0.43 | 1 |