Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs267601867 | 1.000 | 0.080 | 8 | 24465702 | missense variant | C/G;T | snv | 1.2E-05 | 1 | ||
rs137990671 | 1.000 | 0.080 | 8 | 24442511 | missense variant | C/A;T | snv | 1 | |||
rs150319320 | 1.000 | 0.080 | 8 | 24441148 | missense variant | C/T | snv | 1 | |||
rs267601868 | 1.000 | 0.080 | 8 | 24487303 | missense variant | G/A | snv | 1 | |||
rs267601866 | 1.000 | 0.080 | 8 | 24442526 | missense variant | C/T | snv | 1 | |||
rs1034941983 | 1.000 | 0.080 | 8 | 24499308 | missense variant | G/A | snv | 1 | |||
rs867202281 | 1.000 | 0.080 | 8 | 24492540 | missense variant | G/A | snv | 7.0E-06 | 1 |