Variant | Gene | DSI v | DPI v | Chr | Position | Consequence | Alleles | Class | AF EXOME | AF GENOME | Num. diseases |
---|---|---|---|---|---|---|---|---|---|---|---|
rs398124401 | 0.695 | 0.480 | 4 | 55346393 | stop gained | G/A | snv | 1.2E-04 | 2.8E-05 | 25 | |
rs28936415 | 0.752 | 0.320 | 16 | 8811153 | missense variant | G/A | snv | 4.1E-03 | 3.7E-03 | 22 | |
rs794727931 | 0.790 | 0.240 | 11 | 78112692 | missense variant | A/C | snv | 19 | |||
rs1164484724 | 0.790 | 0.240 | 9 | 137108433 | stop gained | C/T | snv | 7.0E-06 | 13 | ||
rs913477149 | 0.851 | 0.160 | 3 | 53105728 | missense variant | T/A;C | snv | 13 | |||
rs1555570093 | 0.807 | 0.280 | 17 | 7586699 | missense variant | G/A | snv | 12 | |||
rs376754460 | 0.807 | 0.280 | 16 | 8801859 | missense variant | G/A;C;T | snv | 8.0E-06 | 12 | ||
rs1555493029 | 0.851 | 0.240 | 16 | 23406263 | splice acceptor variant | C/A | snv | 10 | |||
rs1555497604 | 0.851 | 0.240 | 16 | 23452993 | start lost | A/G | snv | 10 | |||
rs1555570110 | 0.827 | 0.240 | 17 | 7586766 | missense variant | A/C | snv | 9 |