Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs768126403 | 1.000 | 0.080 | 13 | 77918517 | stop gained | G/A;T | snv | 4 | |||
rs147682682 | 1.000 | 0.040 | 3 | 69956496 | stop gained | G/A;T | snv | 1.2E-05 | 1.4E-05 | 4 | |
rs1559749017 | 0.925 | 0.040 | 3 | 69956531 | splice donor variant | G/A | snv | 4 | |||
rs773779627 | 1.000 | 0.080 | 20 | 59301689 | missense variant | G/A;T | snv | 4.0E-06 | 5 | ||
rs1561416879 | 0.925 | 0.200 | 5 | 90629308 | stop gained | C/G | snv | 6 | |||
rs104893746 | 0.851 | 0.120 | 3 | 69956460 | stop gained | C/T | snv | 6 | |||
rs1559751245 | 0.882 | 0.280 | 3 | 69959280 | missense variant | C/G | snv | 6 | |||
rs1555565774 | 0.807 | 0.360 | 17 | 44862753 | frameshift variant | G/- | delins | 16 | |||
rs104894396 | 0.672 | 0.400 | 13 | 20189511 | stop gained | C/T | snv | 5.8E-04 | 1.1E-04 | 28 | |
rs368869806 | 0.614 | 0.480 | 9 | 95485875 | splice acceptor variant | C/T | snv | 4.0E-06 | 7.0E-06 | 97 |