Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs2284063 | 0.851 | 0.160 | 22 | 38148291 | non coding transcript exon variant | A/G | snv | 0.40 | 3 | ||
rs738322 | 0.925 | 0.040 | 22 | 38172999 | intron variant | A/G | snv | 0.52 | 2 | ||
rs132985 | 0.827 | 0.120 | 22 | 38167464 | intron variant | C/T | snv | 0.51 | 1 | ||
rs84473 | 1.000 | 0.040 | 22 | 38161319 | intron variant | T/C | snv | 0.52 | 1 | ||
rs132941 | 1.000 | 0.040 | 22 | 38149935 | non coding transcript exon variant | T/A;C | snv | 1 | |||
rs133029 | 22 | 38180308 | intron variant | C/T | snv | 0.11 | 1 | ||||
rs2277844 | 22 | 38181508 | intron variant | G/A | snv | 0.53 | 1 | ||||
rs5756931 | 22 | 38150026 | non coding transcript exon variant | T/A;C | snv | 1 | |||||
rs4608623 | 0.925 | 0.040 | 22 | 38201371 | non coding transcript exon variant | G/T | snv | 0.52 | 1 |