Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs387907201 | 1.000 | 0.080 | 11 | 46739326 | missense variant | G/A;T | snv | 4 | |||
rs1482856709 | 0.925 | 0.080 | 3 | 93900887 | missense variant | G/A | snv | 3 | |||
rs61750610 | 0.925 | 0.080 | 12 | 6013630 | missense variant | G/T | snv | 3 | |||
rs387906691 | 1.000 | 19 | 3595810 | missense variant | C/T | snv | 2 | ||||
rs575627531 | 1.000 | 0.120 | 9 | 104814211 | stop gained | G/A | snv | 2 | |||
rs1339688889 | 12 | 53315733 | missense variant | C/T | snv | 1 |