Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs143683481 | 1.000 | 0.080 | 2 | 26278736 | missense variant | G/A | snv | 9.1E-05 | 3.1E-04 | 1 | |
rs750956714 | 1.000 | 0.080 | 2 | 26277125 | missense variant | T/C | snv | 4.0E-06 | 1 | ||
rs1367079155 | 1.000 | 0.080 | 4 | 99594764 | missense variant | G/C | snv | 4.0E-06 | 1 | ||
rs146064714 | 1.000 | 0.080 | 4 | 99622756 | stop gained | G/T | snv | 1.2E-04 | 3.5E-05 | 1 | |
rs1485375137 | 1.000 | 0.080 | 4 | 99608790 | missense variant | T/C | snv | 7.0E-06 | 1 | ||
rs1553926818 | 1.000 | 0.080 | 4 | 99591735 | frameshift variant | CA/- | delins | 1 | |||
rs1553927840 | 1.000 | 0.080 | 4 | 99608764 | splice acceptor variant | A/G | snv | 1 | |||
rs1560614154 | 1.000 | 0.080 | 4 | 99582057 | frameshift variant | C/- | delins | 1 | |||
rs1560614646 | 1.000 | 0.080 | 4 | 99583431 | stop gained | A/T | snv | 1 | |||
rs1560621444 | 1.000 | 0.080 | 4 | 99601606 | splice acceptor variant | G/A | snv | 1 | |||
rs1560621495 | 1.000 | 0.080 | 4 | 99601674 | missense variant | T/A | snv | 1 | |||
rs199422219 | 1.000 | 0.080 | 4 | 99611156 | stop gained | C/T | snv | 7.0E-06 | 1 | ||
rs199422220 | 1.000 | 0.080 | 4 | 99608827 | missense variant | G/A | snv | 1.6E-05 | 3.5E-05 | 1 | |
rs199422221 | 1.000 | 0.080 | 4 | 99619094 | missense variant | A/T | snv | 1 | |||
rs199422222 | 1.000 | 0.080 | 4 | 99608977 | missense variant | G/T | snv | 1 | |||
rs372321643 | 1.000 | 0.080 | 4 | 99608826 | missense variant | C/T | snv | 2.8E-05 | 4.2E-05 | 1 | |
rs755681036 | 1.000 | 0.080 | 4 | 99613134 | frameshift variant | T/- | delins | 1 | |||
rs767833468 | 1.000 | 0.080 | 4 | 99618993 | missense variant | G/A | snv | 4.0E-06 | 1 | ||
rs1210484348 | 0.925 | 0.080 | 9 | 130884973 | missense variant | C/T | snv | 7.0E-06 | 3 |