Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs17235409 | 0.653 | 0.600 | 2 | 218395009 | missense variant | G/A;C | snv | 4.9E-02; 4.1E-06 | 31 | ||
rs371928156 | 1.000 | 0.040 | 5 | 96998084 | missense variant | C/T | snv | 1 | |||
rs759029280 | 1.000 | 0.040 | 11 | 64318339 | missense variant | G/A | snv | 1 | |||
rs1182070141 | 1.000 | 0.040 | 10 | 95351213 | missense variant | G/A | snv | 8.0E-06 | 1 | ||
rs1196010655 | 1.000 | 0.040 | 10 | 95381799 | splice region variant | T/C | snv | 4.1E-06 | 2.8E-05 | 1 | |
rs147257994 | 1.000 | 0.040 | 10 | 95354958 | missense variant | G/A | snv | 1.2E-05 | 2.1E-05 | 1 | |
rs749801396 | 1.000 | 0.040 | 10 | 95384081 | missense variant | C/G | snv | 4.0E-06 | 1 | ||
rs778662842 | 1.000 | 0.040 | 10 | 95384032 | synonymous variant | T/C | snv | 4.0E-06 | 1 |