Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121909091 | 0.851 | 0.120 | 19 | 10798543 | missense variant | C/T | snv | 4 | |||
rs121909092 | 0.882 | 0.120 | 19 | 10793829 | missense variant | G/A | snv | 4 | |||
rs121909089 | 0.882 | 0.120 | 19 | 10793833 | missense variant | G/A;T | snv | 3 | |||
rs121909090 | 0.882 | 0.120 | 19 | 10793832 | missense variant | C/T | snv | 7.0E-06 | 3 | ||
rs121909095 | 0.882 | 0.120 | 19 | 10823862 | missense variant | C/G;T | snv | 3 | |||
rs587783595 | 0.882 | 0.120 | 19 | 10812271 | missense variant | G/A;T | snv | 3 | |||
rs1555715869 | 0.925 | 0.120 | 19 | 10823859 | missense variant | C/A | snv | 2 | |||
rs587783597 | 0.925 | 0.080 | 19 | 10823868 | missense variant | T/C | snv | 2 | |||
rs587783598 | 0.925 | 0.080 | 19 | 10823886 | missense variant | C/G | snv | 2 | |||
rs121434509 | 1.000 | 0.080 | 3 | 9684627 | missense variant | G/A | snv | 8.0E-06 | 2 | ||
rs121434510 | 1.000 | 0.080 | 3 | 9689034 | missense variant | A/G | snv | 8.0E-06 | 2.1E-05 | 2 | |
rs587783596 | 1.000 | 0.080 | 19 | 10812273 | missense variant | A/C;G | snv | 1 | |||
rs879254086 | 1.000 | 0.080 | 19 | 10819986 | missense variant | G/A | snv | 1 |