Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs4148323 | 0.701 | 0.440 | 2 | 233760498 | missense variant | G/A | snv | 2.2E-02 | 9.2E-03 | 22 | |
rs3755319 | 0.925 | 0.120 | 2 | 233758936 | intron variant | A/C;G;T | snv | 8 | |||
rs34993780 | 0.827 | 0.120 | 2 | 233772413 | missense variant | T/A;C;G | snv | 2.2E-04 | 7 | ||
rs34946978 | 0.851 | 0.120 | 2 | 233768226 | missense variant | C/G;T | snv | 1.2E-03 | 6 |