Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs1057519874 | 0.807 | 0.120 | 7 | 6387261 | missense variant | C/A;T | snv | 4 | |||
rs1057519948 | 0.851 | 0.120 | 7 | 6387262 | missense variant | C/T | snv | 4 | |||
rs1554263624 | 0.925 | 0.120 | 7 | 6391932 | missense variant | A/G | snv | 1 | |||
rs1554263625 | 1.000 | 7 | 6391967 | missense variant | G/A;C | snv | 1 | ||||
rs1554264268 | 0.925 | 0.120 | 7 | 6402337 | missense variant | G/A | snv | 1 | |||
rs1554263626 | 1.000 | 7 | 6392006 | missense variant | T/G | snv | 1 | ||||
rs1554263326 | 1.000 | 7 | 6387229 | missense variant | G/A | snv | 1 |