Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1338204934 | 1.000 | 7 | 100633005 | missense variant | T/C | snv | 7.0E-06 | 1 | |||
rs782010418 | 1.000 | 1 | 146018174 | missense variant | T/A;C | snv | 4.0E-06; 4.0E-06 | 1 | |||
rs1800562 | 0.435 | 0.880 | 6 | 26092913 | missense variant | G/A | snv | 3.3E-02 | 3.8E-02 | 262 |