Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs6742078 | 0.807 | 0.240 | 2 | 233763993 | intron variant | G/T | snv | 0.36 | 13 | ||
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 |