Source: ALL
Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121434287 | 1.000 | 0.080 | 8 | 144415295 | missense variant | G/A | snv | 1.3E-04 | 1.4E-04 | 1 | |
rs121434288 | 1.000 | 0.080 | 8 | 144413288 | missense variant | C/T | snv | 1 | |||
rs121434289 | 1.000 | 0.080 | 8 | 144414291 | missense variant | C/T | snv | 2.1E-05 | 2.1E-05 | 1 | |
rs121434290 | 1.000 | 0.080 | 8 | 144415966 | missense variant | G/T | snv | 1 | |||
rs121434291 | 1.000 | 0.080 | 8 | 144414422 | missense variant | C/T | snv | 1 | |||
rs121434293 | 1.000 | 0.080 | 8 | 144414792 | missense variant | C/G | snv | 1 | |||
rs1871534 | 1.000 | 0.080 | 8 | 144414297 | missense variant | C/G | snv | 0.76 | 1 | ||
rs2977838 | 1.000 | 0.080 | 8 | 144415027 | missense variant | G/A | snv | 3.2E-02 | 1 | ||
rs782110796 | 1.000 | 0.080 | 8 | 144414775 | missense variant | C/T | snv | 8.0E-06 | 1 | ||
rs121434292 | 0.925 | 0.120 | 8 | 144416001 | missense variant | G/A;T | snv | 9.9E-06 | 2 | ||
rs534850657 | 0.925 | 0.120 | 8 | 144413980 | missense variant | A/G | snv | 2 | |||
rs782427403 | 0.925 | 0.120 | 8 | 144413980 | frameshift variant | A/- | del | 4.2E-06 | 7.0E-06 | 2 |