Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs104894972 | 0.807 | 0.240 | Y | 2787320 | missense variant | C/T | snv | 6 | |||
rs104894966 | 0.882 | 0.200 | Y | 2787267 | missense variant | C/T | snv | 3 | |||
rs104894971 | 0.882 | 0.200 | Y | 2787551 | missense variant | C/T | snv | 4.4E-05 | 3 | ||
rs104894959 | 0.925 | 0.160 | Y | 2787334 | missense variant | G/C | snv | 1.5E-05 | 2 | ||
rs104894974 | 0.925 | 0.160 | Y | 2787321 | missense variant | C/G | snv | 2 | |||
rs1556370543 | 0.925 | 0.160 | Y | 2787273 | stop gained | G/A | snv | 2 | |||
rs104894956 | 1.000 | 0.160 | Y | 2787278 | missense variant | A/G | snv | 1 | |||
rs104894957 | 1.000 | 0.160 | Y | 2787426 | missense variant | C/G | snv | 1 | |||
rs104894958 | 1.000 | 0.160 | Y | 2787327 | stop gained | G/A | snv | 1 | |||
rs104894964 | 1.000 | 0.160 | Y | 2787287 | missense variant | T/A | snv | 1 | |||
rs104894965 | 1.000 | 0.160 | Y | 2787395 | stop gained | C/T | snv | 1 | |||
rs104894967 | 1.000 | 0.160 | Y | 2787284 | stop gained | C/T | snv | 1 | |||
rs104894968 | 1.000 | 0.160 | Y | 2787401 | missense variant | A/G | snv | 1 | |||
rs104894969 | 1.000 | 0.160 | Y | 2787412 | missense variant | C/T | snv | 1 | |||
rs104894970 | 1.000 | 0.160 | Y | 2787330 | stop gained | T/A | snv | 1 | |||
rs104894973 | 1.000 | 0.160 | Y | 2787224 | missense variant | T/A;C | snv | 1 | |||
rs104894975 | 1.000 | 0.160 | Y | 2787592 | stop gained | A/T | snv | 1 | |||
rs104894976 | 1.000 | 0.160 | Y | 2787207 | missense variant | G/A | snv | 1 | |||
rs104894977 | 1.000 | 0.160 | Y | 2787600 | stop gained | G/A | snv | 1 | |||
rs1057519627 | 1.000 | 0.160 | Y | 2787377 | missense variant | C/A | snv | 1 | |||
rs1556370548 | 1.000 | 0.160 | Y | 2787316 | stop gained | G/C | snv | 1 | |||
rs1556370556 | 1.000 | 0.160 | Y | 2787339 | frameshift variant | -/T | delins | 1 | |||
rs1556370558 | 1.000 | 0.160 | Y | 2787341 | stop gained | G/T | snv | 1 | |||
rs1556370576 | 1.000 | 0.160 | Y | 2787515 | missense variant | C/A | snv | 1 | |||
rs606231178 | 1.000 | 0.160 | Y | 2787237 | frameshift variant | CTCT/- | delins | 1 |