Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1560814874 | 4 | 143528006 | missense variant | A/C | snv | 1 | |||||
rs1562005199 | 6 | 69382853 | missense variant | G/A | snv | 1 | |||||
rs1562137453 | 6 | 69049307 | missense variant | T/C | snv | 1 | |||||
rs1562308994 | 6 | 99446205 | missense variant | T/C | snv | 1 | |||||
rs1562391520 | 6 | 99482871 | missense variant | C/T | snv | 1 | |||||
rs1562456317 | 6 | 99508705 | missense variant | A/C | snv | 1 | |||||
rs1563293555 | 8 | 42930130 | missense variant | T/G | snv | 1 | |||||
rs1563765580 | 8 | 92017274 | frameshift variant | -/A | ins | 1 | |||||
rs1564726619 | 10 | 69232838 | missense variant | G/T | snv | 1 | |||||
rs1565117343 | 11 | 59594048 | stop gained | G/A | snv | 1 | |||||
rs1565272952 | 11 | 17145862 | splice donor variant | C/A | snv | 1 | |||||
rs1565798439 | 12 | 71610513 | missense variant | A/G | snv | 1 | |||||
rs1566529937 | 13 | 114052075 | missense variant | A/G | snv | 1 | |||||
rs1566615893 | 14 | 24155442 | missense variant | A/G | snv | 1 | |||||
rs1567280099 | 16 | 4697038 | frameshift variant | -/G | delins | 1 | |||||
rs1567547614 | 16 | 30668622 | missense variant | G/A | snv | 1 | |||||
rs1567858976 | 17 | 32477518 | splice region variant | CAGA/- | delins | 1 | |||||
rs1567966432 | 18 | 21383629 | missense variant | T/G | snv | 1 | |||||
rs1568105562 | 17 | 44559091 | missense variant | T/G | snv | 1 | |||||
rs1568162263 | 17 | 40029767 | missense variant | G/C | snv | 1 | |||||
rs1568383758 | 19 | 15255488 | missense variant | C/A | snv | 1 | |||||
rs1569148952 | X | 37991160 | frameshift variant | TG/- | del | 1 | |||||
rs1569197778 | X | 55488927 | stop gained | G/A | snv | 1 | |||||
rs1569405174 | X | 110317618 | frameshift variant | G/- | delins | 1 | |||||
rs193922466 | Y | 634687 | missense variant | A/G | snv | 1 |