Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs121912893 | 0.708 | 0.400 | 12 | 47983721 | stop gained | G/A;T | snv | 15 | |||
rs121912874 | 0.716 | 0.400 | 12 | 47978329 | missense variant | G/A | snv | 14 | |||
rs794727261 | 0.716 | 0.400 | 12 | 47999953 | stop gained | G/T | snv | 14 | |||
rs760093841 | 1.000 | 12 | 47975548 | missense variant | C/A;G;T | snv | 4.1E-06 | 1 | |||
rs869312907 | 0.925 | 0.040 | 12 | 47995910 | missense variant | C/T | snv | 1 |