Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs375002796 | 0.851 | 0.160 | 7 | 76058047 | missense variant | C/T | snv | 5.2E-05 | 2.8E-05 | 7 | |
rs796052676 | 0.807 | 0.200 | 8 | 132180246 | missense variant | G/A | snv | 7 | |||
rs61748421 | 0.807 | 0.200 | X | 154031326 | stop gained | G/A;T | snv | 6 | |||
rs1057518786 | 1.000 | 6 | 33441374 | splice region variant | G/A | snv | 5 | ||||
rs1057519444 | 0.925 | 0.120 | 22 | 32518208 | missense variant | GG/AA | mnv | 5 | |||
rs1057519567 | 0.882 | 0.040 | 7 | 76063554 | frameshift variant | G/- | delins | 5 | |||
rs1131692228 | 0.925 | 0.160 | 7 | 100646637 | missense variant | C/T | snv | 5 | |||
rs377619533 | 1.000 | 18 | 33743312 | stop gained | C/A;T | snv | 2.8E-05 | 5 | |||
rs587777623 | 0.882 | 0.120 | 11 | 686986 | missense variant | G/A | snv | 4.0E-06 | 5 | ||
rs145999922 | 0.882 | 0.040 | 2 | 227699378 | missense variant | A/G | snv | 4.4E-05 | 4.2E-05 | 4 | |
rs397514627 | 0.882 | 0.160 | 10 | 73842486 | missense variant | C/A;G | snv | 4 | |||
rs750371878 | 0.925 | 6 | 104796666 | stop gained | G/A | snv | 4.0E-06 | 1.4E-05 | 4 | ||
rs775835429 | 0.925 | 0.040 | 2 | 227702236 | frameshift variant | -/TC | delins | 2.4E-05 | 2.1E-05 | 4 | |
rs1555736565 | 0.925 | 0.080 | 19 | 13230191 | missense variant | C/A;T | snv | 3 | |||
rs778899140 | 0.925 | 6 | 165450268 | missense variant | T/C | snv | 4.0E-06 | 3 |