Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs894151 | 1.000 | 0.080 | 8 | 95226180 | intron variant | T/C | snv | 0.39 | 2 | ||
rs9926344 | 1.000 | 0.080 | 16 | 78986883 | intron variant | G/A;C;T | snv | 2 | |||
rs553717 | 13 | 91693325 | missense variant | C/T | snv | 0.14 | 0.14 | 1 | |||
rs778264641 | 7 | 127686719 | missense variant | G/A | snv | 1 | |||||
rs984502020 | 3 | 119807429 | missense variant | G/C | snv | 1 | |||||
rs747489687 | 0.925 | 0.080 | 8 | 6444626 | frameshift variant | AAGAAATATTGCA/- | delins | 2.3E-04 | 1.0E-04 | 4 | |
rs121913377 | 0.354 | 0.840 | 7 | 140753335 | missense variant | CA/AT;TT | mnv | 480 | |||
rs1057519855 | 0.776 | 0.120 | 11 | 533873 | missense variant | CT/AC;TC | mnv | 11 |