Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs61863282 | 10 | 97591247 | intron variant | C/T | snv | 0.11 | 1 | ||||
rs11817730 | 10 | 97598754 | intron variant | A/G | snv | 0.18 | 0.20 | 1 | |||
rs2297644 | 10 | 97599982 | non coding transcript exon variant | T/C | snv | 0.15 | 1 | ||||
rs7068278 | 10 | 97597385 | intron variant | G/T | snv | 0.18 | 1 | ||||
rs7078003 | 10 | 97599655 | non coding transcript exon variant | C/T | snv | 0.14 | 0.14 | 1 | |||
rs7913812 | 10 | 97597874 | intron variant | T/C | snv | 0.20 | 1 | ||||
rs2861970 | 10 | 97592327 | intron variant | A/C;G;T | snv | 1 |